Linked Data
ClinVar Variation Id:
525570
dbSNP Id:
rs201925425
ExAC:
17:72308276 G / A
gnomAD v2:
17-72308276-G-A
gnomAD v3:
17-74312137-G-A
gnomAD v4:
17-74312137-G-A
COSMIC:
COSM3403187
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.74312137G>A , CM000679.2:g.74312137G>A | GRCh38 |
| NC_000017.10:g.72308276G>A , CM000679.1:g.72308276G>A | GRCh37 |
| NC_000017.9:g.69819871G>A | NCBI36 |
| NG_016865.1:g.42891G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311014.11:c.1629G>A MANE Select | ENSP00000308312.6:p.Ala543= | |
| ENST00000311014.10:c.1629G>A | ENSP00000308312.6:p.Ala543= | |
| ENST00000446837.2:c.1629G>A | ENSP00000400252.2:p.Ala543= | |
| ENST00000579055.5:c.*938+62G>A | ENSP00000462767.1:n.*938+62G>A | |
| ENST00000579490.5:c.1800G>A | ENSP00000464197.1:p.Ala600= | |
| ENST00000582036.5:c.1593G>A | ENSP00000461950.1:p.Ala531= | |
| NM_001172810.1:c.1593G>A | NP_001166281.1:p.Ala531= | |
| NM_023036.4:c.1629G>A | NP_075462.3:p.Ala543= | |
| XM_011525125.1:c.1629G>A | XP_011523427.1:p.Ala543= | |
| XR_429915.2:n.1715G>A | ||
| XR_429916.2:n.1616+1974G>A | ||
| XR_934518.1:n.1753G>A | ||
| XR_934519.1:n.1750G>A | ||
| XR_934520.1:n.1826G>A | ||
| XR_934521.1:n.1738G>A | ||
| XR_934522.1:n.1726G>A | ||
| XR_934523.1:n.1735G>A | ||
| XR_934524.1:n.1753G>A | ||
| XR_934525.1:n.1717G>A | ||
| XR_934526.1:n.1639G>A | ||
| XR_934527.1:n.1689+62G>A | ||
| XR_934528.1:n.1689+62G>A | ||
| XR_934529.1:n.1632G>A | ||
| XR_934530.1:n.1705G>A | ||
| XR_934531.1:n.1569+62G>A | ||
| XR_934970.1:n.468C>T | ||
| XR_934971.1:n.302C>T | ||
| NM_001172810.2:c.1593G>A | NP_001166281.1:p.Ala531= | |
| NM_001353167.1:c.1629G>A | NP_001340096.1:p.Ala543= | |
| NM_023036.5:c.1629G>A | NP_075462.3:p.Ala543= | |
| NR_148379.1:n.1592+62G>A | ||
| XM_011525125.2:c.1629G>A | XP_011523427.1:p.Ala543= | |
| XM_024450874.1:c.1629G>A | XP_024306642.1:p.Ala543= | |
| XM_024450875.1:c.1629G>A | XP_024306643.1:p.Ala543= | |
| XM_024450876.1:c.1629G>A | XP_024306644.1:p.Ala543= | |
| XM_024450877.1:c.1629G>A | XP_024306645.1:p.Ala543= | |
| XM_024450878.1:c.1629G>A | XP_024306646.1:p.Ala543= | |
| XM_024450879.1:c.1629G>A | XP_024306647.1:p.Ala543= | |
| XM_024450880.1:c.1593G>A | XP_024306648.1:p.Ala531= | |
| XM_024450881.1:c.1515G>A | XP_024306649.1:p.Ala505= | |
| XM_024450882.1:c.1593G>A | XP_024306650.1:p.Ala531= | |
| XM_024450883.1:c.1567+62G>A | XP_024306651.1:n.1567+62G>A | |
| XM_024450884.1:c.1567+62G>A | XP_024306652.1:n.1567+62G>A | |
| XM_024450885.1:c.1200G>A | XP_024306653.1:p.Ala400= | |
| XM_024450886.1:c.1200G>A | XP_024306654.1:p.Ala400= | |
| XR_934970.2:n.472C>T | ||
| XR_934971.2:n.307C>T | ||
| NM_023036.6:c.1629G>A MANE Select | NP_075462.3:p.Ala543= | |
| NM_001172810.3:c.1593G>A | NP_001166281.1:p.Ala531= | |
| NM_001353167.2:c.1629G>A | NP_001340096.1:p.Ala543= | |
| NR_148379.2:n.1568+62G>A |