Linked Data
ClinVar Variation Id:
436062
dbSNP Id:
rs1406037834
gnomAD v2:
5-176638667-T-A
gnomAD v3:
5-177211666-T-A
gnomAD v4:
5-177211666-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.177211666T>A , CM000667.2:g.177211666T>A | GRCh38 |
| NC_000005.9:g.176638667T>A , CM000667.1:g.176638667T>A | GRCh37 |
| NC_000005.8:g.176571273T>A | NCBI36 |
| NG_009821.1:g.83588T>A , LRG_512:g.83588T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000508896.7:c.2394T>A | ENSP00000423372.3:p.Asp798Glu | |
| ENST00000347982.9:c.2394T>A | ENSP00000343209.5:p.Asp798Glu | |
| ENST00000354179.9:c.2394T>A | ENSP00000346111.5:p.Asp798Glu | |
| ENST00000510954.6:n.612+7374T>A | ||
| ENST00000685206.1:n.2850T>A | ||
| ENST00000686993.1:c.2394T>A | ENSP00000510020.1:p.Asp798Glu | |
| ENST00000687453.1:c.2958T>A | ENSP00000508426.1:p.Asp986Glu | |
| ENST00000688613.1:n.2664T>A | ||
| ENST00000689326.1:c.3267T>A | ENSP00000509594.1:p.Asp1089Glu | |
| ENST00000689345.1:c.2394T>A | ENSP00000509711.1:p.Asp798Glu | |
| ENST00000689549.1:n.3414T>A | ||
| ENST00000439151.7:c.3267T>A MANE Select | ENSP00000395929.2:p.Asp1089Glu | |
| ENST00000347982.8:c.2460T>A | ENSP00000343209.4:p.Asp820Glu | |
| ENST00000354179.8:c.2460T>A | ENSP00000346111.4:p.Asp820Glu | |
| ENST00000439151.6:c.3267T>A | ENSP00000395929.2:p.Asp1089Glu | |
| NM_022455.4:c.3267T>A , LRG_512t1:c.3267T>A | NP_071900.2:p.Asp1089Glu | |
| NM_172349.2:c.2460T>A | NP_758859.1:p.Asp820Glu | |
| XM_005265959.1:c.3267T>A | XP_005266016.1:p.Asp1089Glu | |
| XM_005265960.1:c.2460T>A | XP_005266017.1:p.Asp820Glu | |
| XM_005265961.1:c.2460T>A | XP_005266018.1:p.Asp820Glu | |
| XM_011534610.1:c.3267T>A | XP_011532912.1:p.Asp1089Glu | |
| XM_011534611.1:c.3267T>A | XP_011532913.1:p.Asp1089Glu | |
| XM_011534612.1:c.2847T>A | XP_011532914.1:p.Asp949Glu | |
| XM_011534613.1:c.2211T>A | XP_011532915.1:p.Asp737Glu | |
| XM_011534614.1:c.3267T>A | XP_011532916.1:p.Asp1089Glu | |
| XM_011534615.1:c.3267T>A | XP_011532917.1:p.Asp1089Glu | |
| XM_011534616.1:c.3267T>A | XP_011532918.1:p.Asp1089Glu | |
| NM_001365684.1:c.2460T>A | NP_001352613.1:p.Asp820Glu | |
| XM_024446150.1:c.3267T>A | XP_024301918.1:p.Asp1089Glu | |
| XM_024446151.1:c.3267T>A | XP_024301919.1:p.Asp1089Glu | |
| XM_024446152.1:c.3267T>A | XP_024301920.1:p.Asp1089Glu | |
| XM_024446153.1:c.3267T>A | XP_024301921.1:p.Asp1089Glu | |
| XM_024446154.1:c.2847T>A | XP_024301922.1:p.Asp949Glu | |
| XM_024446155.1:c.2460T>A | XP_024301923.1:p.Asp820Glu | |
| XM_024446156.1:c.2460T>A | XP_024301924.1:p.Asp820Glu | |
| XM_024446158.1:c.2460T>A | XP_024301926.1:p.Asp820Glu | |
| XM_024446159.1:c.2211T>A | XP_024301927.1:p.Asp737Glu | |
| XM_024446160.1:c.3267T>A | XP_024301928.1:p.Asp1089Glu | |
| XM_024446161.1:c.3267T>A | XP_024301929.1:p.Asp1089Glu | |
| XM_024446162.1:c.-729T>A | XP_024301930.1:n.-729T>A | |
| NM_022455.5:c.3267T>A MANE Select | NP_071900.2:p.Asp1089Glu | |
| NM_172349.3:c.2460T>A | NP_758859.1:p.Asp820Glu |