SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.88610915T>A , CM000676.2:g.88610915T>A | GRCh38 |
| NC_000014.8:g.89077259T>A , CM000676.1:g.89077259T>A | GRCh37 |
| NC_000014.7:g.88147012T>A | NCBI36 |
| NG_050601.1:g.53007T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251038.10:c.2179T>A MANE Select | ENSP00000251038.5:p.Leu727Met | |
| ENST00000649731.1:c.*1387T>A | ENSP00000497757.1:n.*1387T>A | |
| ENST00000251038.9:c.2179T>A | ENSP00000251038.5:p.Leu727Met | |
| ENST00000302216.12:c.1708T>A | ENSP00000307025.8:p.Leu570Met | |
| ENST00000318308.10:c.889T>A | ENSP00000327176.6:p.Leu297Met | |
| ENST00000336693.8:c.1684T>A | ENSP00000338002.4:p.Leu562Met | |
| ENST00000393514.9:c.2104T>A | ENSP00000377150.5:p.Leu702Met | |
| ENST00000406216.7:c.817T>A | ENSP00000384682.3:p.Leu273Met | |
| ENST00000554020.5:n.1022T>A | ||
| ENST00000555755.5:c.2161T>A | ENSP00000452475.1:p.Leu721Met | |
| ENST00000555792.1:c.424T>A | ENSP00000450823.1:p.Leu142Met | |
| ENST00000555851.6:n.338T>A | ||
| ENST00000555900.5:c.1285T>A | ENSP00000451530.1:p.Leu429Met | |
| ENST00000556000.5:c.1923T>A | ||
| ENST00000556945.5:c.1786T>A | ENSP00000450474.1:p.Leu596Met | |
| ENST00000557491.1:n.1464T>A | ||
| ENST00000557607.5:c.1231T>A | ENSP00000452370.1:p.Leu411Met | |
| NM_001160103.1:c.2176T>A | NP_001153575.1:p.Leu726Met | |
| NM_001160104.1:c.2161T>A | NP_001153576.1:p.Leu721Met | |
| NM_024824.4:c.2179T>A | NP_079100.2:p.Leu727Met | |
| NM_207660.3:c.1708T>A | NP_997543.1:p.Leu570Met | |
| NM_207661.2:c.1684T>A | NP_997544.1:p.Leu562Met | |
| NM_207662.3:c.889T>A | NP_997545.2:p.Leu297Met | |
| XM_005268067.3:c.2164T>A | XP_005268124.1:p.Leu722Met | |
| XM_005268068.3:c.2104T>A | XP_005268125.1:p.Leu702Met | |
| XM_005268069.3:c.1786T>A | XP_005268126.1:p.Leu596Met | |
| XM_005268070.3:c.1783T>A | XP_005268127.1:p.Leu595Met | |
| XM_005268071.3:c.1711T>A | XP_005268128.1:p.Leu571Met | |
| XM_005268073.3:c.1285T>A | XP_005268130.1:p.Leu429Met | |
| XM_006720257.2:c.1210T>A | XP_006720320.1:p.Leu404Met | |
| XM_011537160.1:c.2077T>A | XP_011535462.1:p.Leu693Met | |
| XM_011537161.1:c.2023T>A | XP_011535463.1:p.Leu675Met | |
| NM_001326295.1:c.1786T>A | NP_001313224.1:p.Leu596Met | |
| NM_001326296.1:c.2101T>A | NP_001313225.1:p.Leu701Met | |
| NM_001326297.1:c.2077T>A | NP_001313226.1:p.Leu693Met | |
| NM_001326298.1:c.1711T>A | NP_001313227.1:p.Leu571Met | |
| NM_001326299.1:c.2086T>A | NP_001313228.1:p.Leu696Met | |
| NM_001326300.1:c.1714T>A | NP_001313229.1:p.Leu572Met | |
| NM_001326301.1:c.2002T>A | NP_001313230.1:p.Leu668Met | |
| NM_001326302.1:c.1711T>A | NP_001313231.1:p.Leu571Met | |
| NM_001326303.1:c.1606T>A | NP_001313232.1:p.Leu536Met | |
| NM_001326304.1:c.1318T>A | NP_001313233.1:p.Leu440Met | |
| NM_001326305.1:c.1639T>A | NP_001313234.1:p.Leu547Met | |
| NM_001326306.1:c.1552T>A | NP_001313235.1:p.Leu518Met | |
| NM_001326307.1:c.2104T>A | NP_001313236.1:p.Leu702Met | |
| NM_001326308.1:c.1321T>A | NP_001313237.1:p.Leu441Met | |
| NM_001326309.1:c.1246T>A | NP_001313238.1:p.Leu416Met | |
| NM_001326310.1:c.2164T>A | NP_001313239.1:p.Leu722Met | |
| NM_001326311.1:c.1243T>A | NP_001313240.1:p.Leu415Met | |
| NM_001326312.1:c.2089T>A | NP_001313241.1:p.Leu697Met | |
| NM_001326313.1:c.1555T>A | NP_001313242.1:p.Leu519Met | |
| NM_001326314.1:c.1636T>A | NP_001313243.1:p.Leu546Met | |
| NM_001326315.1:c.2074T>A | NP_001313244.1:p.Leu692Met | |
| NM_001326316.1:c.2074T>A | NP_001313245.1:p.Leu692Met | |
| NR_136936.1:n.2244T>A | ||
| XM_005268070.5:c.1783T>A | XP_005268127.1:p.Leu595Met | |
| XM_005268073.4:c.1285T>A | XP_005268130.1:p.Leu429Met | |
| XM_006720257.3:c.1210T>A | XP_006720320.1:p.Leu404Met | |
| XM_011537161.3:c.2023T>A | XP_011535463.1:p.Leu675Met | |
| XM_024449713.1:c.1207T>A | XP_024305481.1:p.Leu403Met | |
| NM_024824.5:c.2179T>A MANE Select | NP_079100.2:p.Leu727Met | |
| NM_001160103.2:c.2176T>A | NP_001153575.1:p.Leu726Met | |
| NM_001160104.2:c.2161T>A | NP_001153576.1:p.Leu721Met | |
| NM_001326295.2:c.1786T>A | NP_001313224.1:p.Leu596Met | |
| NM_001326296.2:c.2101T>A | NP_001313225.1:p.Leu701Met | |
| NM_001326297.2:c.2077T>A | NP_001313226.1:p.Leu693Met | |
| NM_001326298.2:c.1711T>A | NP_001313227.1:p.Leu571Met | |
| NM_001326299.2:c.2086T>A | NP_001313228.1:p.Leu696Met | |
| NM_001326300.2:c.1714T>A | NP_001313229.1:p.Leu572Met | |
| NM_001326301.2:c.2002T>A | NP_001313230.1:p.Leu668Met | |
| NM_001326302.2:c.1711T>A | NP_001313231.1:p.Leu571Met | |
| NM_001326303.2:c.1606T>A | NP_001313232.1:p.Leu536Met | |
| NM_001326304.2:c.1318T>A | NP_001313233.1:p.Leu440Met | |
| NM_001326305.2:c.1639T>A | NP_001313234.1:p.Leu547Met | |
| NM_001326306.2:c.1552T>A | NP_001313235.1:p.Leu518Met | |
| NM_001326307.2:c.2104T>A | NP_001313236.1:p.Leu702Met | |
| NM_001326308.2:c.1321T>A | NP_001313237.1:p.Leu441Met | |
| NM_001326309.2:c.1246T>A | NP_001313238.1:p.Leu416Met | |
| NM_001326310.2:c.2164T>A | NP_001313239.1:p.Leu722Met | |
| NM_001326311.2:c.1243T>A | NP_001313240.1:p.Leu415Met | |
| NM_001326312.2:c.2089T>A | NP_001313241.1:p.Leu697Met | |
| NM_001326313.2:c.1555T>A | NP_001313242.1:p.Leu519Met | |
| NM_001326314.2:c.1636T>A | NP_001313243.1:p.Leu546Met | |
| NM_001326315.2:c.2074T>A | NP_001313244.1:p.Leu692Met | |
| NM_207660.4:c.1708T>A | NP_997543.1:p.Leu570Met | |
| NM_207662.4:c.889T>A | NP_997545.2:p.Leu297Met | |
| NR_136936.2:n.2116T>A | ||
| NM_001326316.2:c.2074T>A | NP_001313245.1:p.Leu692Met | |
| NM_207661.3:c.1684T>A | NP_997544.1:p.Leu562Met |