Linked Data
ClinVar Variation Id:
409404
dbSNP Id:
rs751478971
ExAC:
17:17122419 G / A
gnomAD v2:
17-17122419-G-A
gnomAD v4:
17-17219105-G-A
COSMIC:
COSM3514717
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.17219105G>A , CM000679.2:g.17219105G>A | GRCh38 |
| NC_000017.10:g.17122419G>A , CM000679.1:g.17122419G>A | GRCh37 |
| NC_000017.9:g.17063144G>A | NCBI36 |
| NG_008001.2:g.23084C>T , LRG_325:g.23084C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000285071.9:c.976C>T MANE Select | ENSP00000285071.4:p.Pro326Ser | |
| ENST00000285071.8:c.976C>T | ENSP00000285071.4:p.Pro326Ser | |
| ENST00000427497.3:c.149-51C>T | ENSP00000394249.3:n.149-51C>T | |
| NM_144997.5:c.976C>T , LRG_325t1:c.976C>T | NP_659434.2:p.Pro326Ser | |
| XM_011523714.1:c.1030C>T | XP_011522016.1:p.Pro344Ser | |
| XM_011523715.1:c.1030C>T | XP_011522017.1:p.Pro344Ser | |
| XM_011523716.1:c.1030C>T | XP_011522018.1:p.Pro344Ser | |
| XM_011523717.1:c.1030C>T | XP_011522019.1:p.Pro344Ser | |
| XM_011523718.1:c.1030C>T | XP_011522020.1:p.Pro344Ser | |
| XM_011523719.1:c.1030C>T | XP_011522021.1:p.Pro344Ser | |
| XM_011523720.1:c.754C>T | XP_011522022.1:p.Pro252Ser | |
| XM_011523721.1:c.1030C>T | XP_011522023.1:p.Pro344Ser | |
| XR_934007.1:n.2370C>T | ||
| NM_001353229.1:c.1030C>T | NP_001340158.1:p.Pro344Ser | |
| NM_001353230.1:c.976C>T | NP_001340159.1:p.Pro326Ser | |
| NM_001353231.1:c.976C>T | NP_001340160.1:p.Pro326Ser | |
| NM_144997.6:c.976C>T | NP_659434.2:p.Pro326Ser | |
| XM_011523714.3:c.1030C>T | XP_011522016.1:p.Pro344Ser | |
| XM_011523718.3:c.1030C>T | XP_011522020.1:p.Pro344Ser | |
| XM_011523719.3:c.1030C>T | XP_011522021.1:p.Pro344Ser | |
| XM_011523721.3:c.1030C>T | XP_011522023.1:p.Pro344Ser | |
| XM_017024305.2:c.1030C>T | XP_016879794.1:p.Pro344Ser | |
| XM_017024308.1:c.976C>T | XP_016879797.1:p.Pro326Ser | |
| XM_017024309.2:c.754C>T | XP_016879798.1:p.Pro252Ser | |
| XM_024450635.1:c.1030C>T | XP_024306403.1:p.Pro344Ser | |
| XR_001752445.2:n.1534C>T | ||
| NM_144997.7:c.976C>T MANE Select | NP_659434.2:p.Pro326Ser | |
| NM_001353229.2:c.1030C>T | NP_001340158.1:p.Pro344Ser | |
| NM_001353230.2:c.976C>T | NP_001340159.1:p.Pro326Ser | |
| NM_001353231.2:c.976C>T | NP_001340160.1:p.Pro326Ser |