Canonical Allele Identifier: CA408634782
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443590C>T , CM000682.2:g.33443590C>T GRCh38
NC_000020.10:g.32031396C>T , CM000682.1:g.32031396C>T GRCh37
NC_000020.9:g.31495057C>T NCBI36
NG_011622.1:g.5303G>A , LRG_332:g.5303G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.31G>A MANE Select ENSP00000217381.2:p.Gly11Arg
ENST00000217381.2:c.31G>A ENSP00000217381.2:p.Gly11Arg
NM_003098.2:c.31G>A , LRG_332t1:c.31G>A NP_003089.1:p.Gly11Arg
XM_005260517.1:c.31G>A XP_005260574.1:p.Gly11Arg
XM_011529007.1:c.31G>A XP_011527309.1:p.Gly11Arg
XM_011529008.1:c.31G>A XP_011527310.1:p.Gly11Arg
XR_936612.1:n.264G>A
NM_003098.3:c.31G>A MANE Select NP_003089.1:p.Gly11Arg