Canonical Allele Identifier: CA408634745
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443580T>C , CM000682.2:g.33443580T>C GRCh38
NC_000020.10:g.32031386T>C , CM000682.1:g.32031386T>C GRCh37
NC_000020.9:g.31495047T>C NCBI36
NG_011622.1:g.5313A>G , LRG_332:g.5313A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.41A>G MANE Select ENSP00000217381.2:p.Glu14Gly
ENST00000217381.2:c.41A>G ENSP00000217381.2:p.Glu14Gly
NM_003098.2:c.41A>G , LRG_332t1:c.41A>G NP_003089.1:p.Glu14Gly
XM_005260517.1:c.41A>G XP_005260574.1:p.Glu14Gly
XM_011529007.1:c.41A>G XP_011527309.1:p.Glu14Gly
XM_011529008.1:c.41A>G XP_011527310.1:p.Glu14Gly
XR_936612.1:n.274A>G
NM_003098.3:c.41A>G MANE Select NP_003089.1:p.Glu14Gly