Canonical Allele Identifier: CA408632697
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33417857T>A , CM000682.2:g.33417857T>A GRCh38
NC_000020.10:g.32005663T>A , CM000682.1:g.32005663T>A GRCh37
NC_000020.9:g.31469324T>A NCBI36
NG_011622.1:g.31036A>T , LRG_332:g.31036A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.563A>T MANE Select ENSP00000217381.2:p.Asp188Val
ENST00000217381.2:c.563A>T ENSP00000217381.2:p.Asp188Val
NM_003098.2:c.563A>T , LRG_332t1:c.563A>T NP_003089.1:p.Asp188Val
XM_005260517.1:c.563A>T XP_005260574.1:p.Asp188Val
XM_011529007.1:c.563A>T XP_011527309.1:p.Asp188Val
XM_011529008.1:c.563A>T XP_011527310.1:p.Asp188Val
XR_936612.1:n.796A>T
XM_024451971.1:c.236A>T XP_024307739.1:p.Asp79Val
NM_003098.3:c.563A>T MANE Select NP_003089.1:p.Asp188Val