Canonical Allele Identifier: CA408634785
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443592G>A , CM000682.2:g.33443592G>A GRCh38
NC_000020.10:g.32031398G>A , CM000682.1:g.32031398G>A GRCh37
NC_000020.9:g.31495059G>A NCBI36
NG_011622.1:g.5301C>T , LRG_332:g.5301C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.29C>T MANE Select ENSP00000217381.2:p.Thr10Ile
ENST00000217381.2:c.29C>T ENSP00000217381.2:p.Thr10Ile
NM_003098.2:c.29C>T , LRG_332t1:c.29C>T NP_003089.1:p.Thr10Ile
XM_005260517.1:c.29C>T XP_005260574.1:p.Thr10Ile
XM_011529007.1:c.29C>T XP_011527309.1:p.Thr10Ile
XM_011529008.1:c.29C>T XP_011527310.1:p.Thr10Ile
XR_936612.1:n.262C>T
NM_003098.3:c.29C>T MANE Select NP_003089.1:p.Thr10Ile