Linked Data
ClinVar Variation Id:
98109
dbSNP Id:
rs63750227
gnomAD v3:
14-73217221-G-A
gnomAD v4:
14-73217221-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.73217221G>A , CM000676.2:g.73217221G>A | GRCh38 |
| NC_000014.8:g.73683929G>A , CM000676.1:g.73683929G>A | GRCh37 |
| NC_000014.7:g.72753682G>A | NCBI36 |
| NG_007386.2:g.85751G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000553599.6:c.1213G>A | ENSP00000452477.2:p.Ala405Thr | |
| ENST00000554131.6:c.1225G>A | ENSP00000451915.2:p.Ala409Thr | |
| ENST00000554995.2:n.1975G>A | ||
| ENST00000555386.6:c.*180G>A | ENSP00000450845.1:n.*180G>A | |
| ENST00000556066.2:n.1651G>A | ||
| ENST00000556951.6:c.1213G>A | ENSP00000450551.2:p.Ala405Thr | |
| ENST00000557293.6:c.1105G>A | ENSP00000451880.2:p.Ala369Thr | |
| ENST00000559361.6:c.*1169G>A | ENSP00000454156.1:n.*1169G>A | |
| ENST00000697912.1:c.*413G>A | ENSP00000513477.1:n.*413G>A | |
| ENST00000697913.1:n.6775G>A | ||
| ENST00000697915.1:n.582G>A | ||
| ENST00000700265.1:c.1213G>A | ENSP00000514901.1:p.Ala405Thr | |
| ENST00000700266.1:c.*1437G>A | ENSP00000514902.1:n.*1437G>A | |
| ENST00000700267.1:c.1225G>A | ENSP00000514903.1:p.Ala409Thr | |
| ENST00000700268.1:c.1225G>A | ENSP00000514904.1:p.Ala409Thr | |
| ENST00000700269.1:c.1225G>A | ENSP00000514905.1:p.Ala409Thr | |
| ENST00000700271.1:c.1039G>A | ENSP00000514906.1:p.Ala347Thr | |
| ENST00000700272.1:c.*1169G>A | ENSP00000514907.1:n.*1169G>A | |
| ENST00000700273.1:c.1213G>A | ENSP00000514908.1:p.Ala405Thr | |
| ENST00000700302.1:c.*41G>A | ENSP00000514929.1:n.*41G>A | |
| ENST00000700303.1:c.*887G>A | ENSP00000514930.1:n.*887G>A | |
| ENST00000700304.1:c.*1169G>A | ENSP00000514931.1:n.*1169G>A | |
| ENST00000700305.1:c.*783G>A | ENSP00000514932.1:n.*783G>A | |
| ENST00000700306.1:c.1225G>A | ENSP00000514933.1:p.Ala409Thr | |
| ENST00000700307.1:c.1126G>A | ENSP00000514934.1:p.Ala376Thr | |
| ENST00000700308.1:c.*1169G>A | ENSP00000514935.1:n.*1169G>A | |
| ENST00000700309.1:c.*1314G>A | ENSP00000514936.1:n.*1314G>A | |
| ENST00000700310.1:c.*180G>A | ENSP00000514937.1:n.*180G>A | |
| ENST00000700311.1:c.*41G>A | ENSP00000514938.1:n.*41G>A | |
| ENST00000700312.1:c.976G>A | ENSP00000514939.1:p.Ala326Thr | |
| ENST00000700313.1:c.1213G>A | ENSP00000514940.1:p.Ala405Thr | |
| ENST00000700314.1:c.*1164G>A | ENSP00000514941.1:n.*1164G>A | |
| ENST00000700315.1:c.*783G>A | ENSP00000514942.1:n.*783G>A | |
| ENST00000700316.1:c.*1005G>A | ENSP00000514943.1:n.*1005G>A | |
| ENST00000700317.1:c.1225G>A | ENSP00000514944.1:p.Ala409Thr | |
| ENST00000700318.1:c.*887G>A | ENSP00000514945.1:n.*887G>A | |
| ENST00000700319.1:c.*665G>A | ENSP00000514946.1:n.*665G>A | |
| ENST00000700320.1:c.1252G>A | ENSP00000514947.1:p.Ala418Thr | |
| ENST00000700321.1:c.1225G>A | ENSP00000514948.1:p.Ala409Thr | |
| ENST00000700322.1:c.1213G>A | ENSP00000514949.1:p.Ala405Thr | |
| ENST00000700323.1:c.1225G>A | ENSP00000514950.1:p.Ala409Thr | |
| ENST00000700324.1:c.1213G>A | ENSP00000514951.1:p.Ala405Thr | |
| ENST00000700375.1:c.1225G>A | ENSP00000514966.1:p.Ala409Thr | |
| ENST00000700377.1:c.*693G>A | ENSP00000514967.1:n.*693G>A | |
| ENST00000700378.1:c.1225G>A | ENSP00000514968.1:p.Ala409Thr | |
| ENST00000700379.1:n.1623G>A | ||
| ENST00000700389.1:c.1213G>A | ENSP00000514970.1:p.Ala405Thr | |
| ENST00000700390.1:n.2936G>A | ||
| ENST00000700391.1:n.436G>A | ||
| ENST00000700404.1:n.2224G>A | ||
| ENST00000700436.1:c.*180G>A | ENSP00000514987.1:n.*180G>A | |
| ENST00000700437.1:c.976G>A | ENSP00000514988.1:p.Ala326Thr | |
| ENST00000700468.1:c.1114G>A | ENSP00000515001.1:p.Ala372Thr | |
| ENST00000700469.1:c.1213G>A | ENSP00000515002.1:p.Ala405Thr | |
| ENST00000324501.10:c.1225G>A MANE Select | ENSP00000326366.5:p.Ala409Thr | |
| ENST00000324501.9:c.1225G>A | ENSP00000326366.5:p.Ala409Thr | |
| ENST00000357710.8:c.1213G>A | ENSP00000350342.4:p.Ala405Thr | |
| ENST00000394164.5:c.1213G>A | ENSP00000377719.1:p.Ala405Thr | |
| ENST00000406768.1:c.949G>A | ENSP00000385948.1:p.Ala317Thr | |
| ENST00000555386.5:c.1305G>A | ENSP00000450845.1:n.1305G>A | |
| ENST00000555867.1:n.590G>A | ||
| ENST00000557511.5:c.1051G>A | ENSP00000451429.1:p.Ala351Thr | |
| NM_000021.3:c.1225G>A | NP_000012.1:p.Ala409Thr | |
| NM_007318.2:c.1213G>A | NP_015557.2:p.Ala405Thr | |
| XM_005267864.1:c.1225G>A | XP_005267921.1:p.Ala409Thr | |
| XM_005267866.1:c.1213G>A | XP_005267923.1:p.Ala405Thr | |
| XM_011536971.1:c.1225G>A | XP_011535273.1:p.Ala409Thr | |
| XM_011536972.1:c.1225G>A | XP_011535274.1:p.Ala409Thr | |
| XM_011536973.1:c.1213G>A | XP_011535275.1:p.Ala405Thr | |
| XM_011536974.1:c.1213G>A | XP_011535276.1:p.Ala405Thr | |
| XM_005267864.3:c.1225G>A | XP_005267921.1:p.Ala409Thr | |
| XM_005267866.2:c.1213G>A | XP_005267923.1:p.Ala405Thr | |
| XM_011536972.2:c.1225G>A | XP_011535274.1:p.Ala409Thr | |
| XM_011536973.2:c.1213G>A | XP_011535275.1:p.Ala405Thr | |
| XM_011536974.2:c.1213G>A | XP_011535276.1:p.Ala405Thr | |
| NM_000021.4:c.1225G>A MANE Select | NP_000012.1:p.Ala409Thr | |
| NM_007318.3:c.1213G>A | NP_015557.2:p.Ala405Thr |