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.
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.127938783C= , CM000666.2:g.127938783C= | GRCh38 |
| NC_000004.11:g.128859938C= , CM000666.1:g.128859938C= | GRCh37 |
| NC_000004.10:g.129079388C= | NCBI36 |
| NG_008657.1:g.32202G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296468.8:c.754G= | ENSP00000296468.3:p.Ala252= | |
| ENST00000505284.6:n.970G= | ||
| ENST00000509826.2:c.698+1070G= | ENSP00000421176.2:n.698+1070G= | |
| ENST00000513559.6:c.472G= | ENSP00000425000.2:p.Ala158= | |
| ENST00000515130.6:c.619G= | ENSP00000493056.1:p.Ala207= | |
| ENST00000641025.1:c.754G= | ENSP00000493346.1:p.Ala252= | |
| ENST00000641092.1:c.553+3262G= | ENSP00000493392.1:n.553+3262G= | |
| ENST00000641133.1:c.*68G= | ENSP00000493192.1:n.*68G= | |
| ENST00000641134.1:c.474G= | ENSP00000492925.1:p.Lys158= | |
| ENST00000641147.1:c.304+4969G= | ENSP00000493133.1:n.304+4969G= | |
| ENST00000641178.1:c.619G= | ENSP00000492989.1:p.Ala207= | |
| ENST00000641186.1:c.640G= | ENSP00000493347.1:p.Ala214= | |
| ENST00000641228.1:c.553+3262G= | ENSP00000493194.1:n.553+3262G= | |
| ENST00000641243.1:c.609G= | ENSP00000493083.1:p.Lys203= | |
| ENST00000641264.1:c.*551G= | ENSP00000492908.1:n.*551G= | |
| ENST00000641332.1:c.609G= | ENSP00000493397.1:p.Lys203= | |
| ENST00000641340.1:c.698+1070G= | ENSP00000493191.1:n.698+1070G= | |
| ENST00000641369.1:c.250G= | ENSP00000493037.1:p.Ala84= | |
| ENST00000641393.1:c.304+4969G= | ENSP00000493197.1:n.304+4969G= | |
| ENST00000641397.1:c.439+4969G= | ENSP00000493406.1:n.439+4969G= | |
| ENST00000641434.1:c.754G= | ENSP00000493279.1:p.Ala252= | |
| ENST00000641464.1:c.449+1070G= | ENSP00000493438.1:n.449+1070G= | |
| ENST00000641482.1:c.754G= | ENSP00000493277.1:p.Ala252= | |
| ENST00000641503.1:c.640G= | ENSP00000493304.1:p.Ala214= | |
| ENST00000641508.1:c.698+1070G= | ENSP00000493209.1:n.698+1070G= | |
| ENST00000641509.1:c.439+4969G= | ENSP00000493459.1:n.439+4969G= | |
| ENST00000641538.1:c.600G= | ||
| ENST00000641590.1:c.640G= | ENSP00000493132.1:p.Ala214= | |
| ENST00000641658.1:c.474G= | ENSP00000492987.1:p.Lys158= | |
| ENST00000641686.2:c.754G= MANE Select | ENSP00000493218.2:p.Ala252= | |
| ENST00000641690.1:c.553+3262G= | ENSP00000492966.1:n.553+3262G= | |
| ENST00000641695.1:c.*38G= | ENSP00000493134.1:n.*38G= | |
| ENST00000641742.1:c.609G= | ENSP00000493315.1:p.Lys203= | |
| ENST00000641743.1:c.754G= | ENSP00000493130.1:p.Ala252= | |
| ENST00000641748.1:c.754G= | ENSP00000493330.1:p.Ala252= | |
| ENST00000641753.1:c.581G= | ||
| ENST00000641774.1:c.584+1070G= | ENSP00000492960.1:n.584+1070G= | |
| ENST00000641776.1:c.*306G= | ENSP00000493261.1:n.*306G= | |
| ENST00000641830.1:c.90G= | ||
| ENST00000641843.1:c.360G= | ENSP00000493174.1:p.Lys120= | |
| ENST00000641869.1:c.59G= | ||
| ENST00000641870.1:c.609G= | ENSP00000493044.1:p.Lys203= | |
| ENST00000641882.1:c.495G= | ENSP00000493301.1:p.Lys165= | |
| ENST00000641928.1:c.449+1070G= | ENSP00000493418.1:n.449+1070G= | |
| ENST00000641949.1:c.553+3262G= | ENSP00000492891.1:n.553+3262G= | |
| ENST00000642012.1:n.618G= | ||
| ENST00000642034.1:c.640G= | ENSP00000493285.1:p.Ala214= | |
| ENST00000642042.1:c.754G= | ENSP00000493260.1:p.Ala252= | |
| ENST00000642078.1:c.474G= | ENSP00000492885.1:p.Lys158= | |
| ENST00000642121.1:n.91-7966G= | ||
| ENST00000296468.7:c.754G= | ENSP00000296468.3:p.Ala252= | |
| ENST00000505284.5:n.649G= | ||
| ENST00000508441.1:n.621G= | ||
| ENST00000509826.1:c.449+1070G= | ENSP00000421176.1:n.449+1070G= | |
| ENST00000513559.5:c.619G= | ENSP00000425000.1:p.Ala207= | |
| ENST00000515130.5:n.1200G= | ||
| NM_152778.2:c.754G= | NP_689991.1:p.Ala252= | |
| XM_005262893.1:c.754G= | XP_005262950.1:p.Ala252= | |
| XM_005262896.1:c.607G= | XP_005262953.1:p.Ala203= | |
| XM_005262897.1:c.553+3262G= | XP_005262954.1:n.553+3262G= | |
| XM_005262898.2:c.754G= | XP_005262955.1:p.Ala252= | |
| XM_005262900.2:c.609G= | XP_005262957.1:p.Lys203= | |
| XM_011531830.1:c.640G= | XP_011530132.1:p.Ala214= | |
| XM_011531831.1:c.439+4969G= | XP_011530133.1:n.439+4969G= | |
| XM_011531832.1:c.640G= | XP_011530134.1:p.Ala214= | |
| XR_938717.1:n.831G= | ||
| NM_001363520.1:c.553+3262G= | NP_001350449.1:n.553+3262G= | |
| NM_001363521.1:c.439+4969G= | NP_001350450.1:n.439+4969G= | |
| XM_005262898.3:c.754G= | XP_005262955.1:p.Ala252= | |
| XM_017007989.1:c.553+3262G= | XP_016863478.1:n.553+3262G= | |
| XM_024453981.1:c.619G= | XP_024309749.1:p.Ala207= | |
| XM_024453982.1:c.505G= | XP_024309750.1:p.Ala169= | |
| XM_024453983.1:c.304+4969G= | XP_024309751.1:n.304+4969G= | |
| XR_001741194.1:n.831G= | ||
| XR_001741195.1:n.717G= | ||
| XR_001741196.1:n.630+3262G= | ||
| XR_001741197.1:n.686G= | ||
| XR_001741198.2:n.686G= | ||
| XR_001741199.1:n.686G= | ||
| XR_938717.2:n.831G= | ||
| NM_001363520.2:c.553+3262G= | NP_001350449.1:n.553+3262G= | |
| NM_001363521.2:c.439+4969G= | NP_001350450.1:n.439+4969G= | |
| NM_001371590.1:c.619G= | NP_001358519.1:p.Ala207= | |
| NM_001371591.1:c.754G= | NP_001358520.1:p.Ala252= | |
| NM_001371592.1:c.760G= | NP_001358521.1:p.Ala254= | |
| NM_001371593.1:c.640G= | NP_001358522.1:p.Ala214= | |
| NM_001371594.1:c.607G= | NP_001358523.1:p.Ala203= | |
| NM_001371595.1:c.472G= | NP_001358524.1:p.Ala158= | |
| NM_001371596.2:c.754G= MANE Select | NP_001358525.1:p.Ala252= | |
| NM_152778.3:c.754G= | NP_689991.1:p.Ala252= | |
| NM_152778.4:c.754G= | NP_689991.1:p.Ala252= |