Canonical Allele Identifier: CA408634789
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443593T>A , CM000682.2:g.33443593T>A GRCh38
NC_000020.10:g.32031399T>A , CM000682.1:g.32031399T>A GRCh37
NC_000020.9:g.31495060T>A NCBI36
NG_011622.1:g.5300A>T , LRG_332:g.5300A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.28A>T MANE Select ENSP00000217381.2:p.Thr10Ser
ENST00000217381.2:c.28A>T ENSP00000217381.2:p.Thr10Ser
NM_003098.2:c.28A>T , LRG_332t1:c.28A>T NP_003089.1:p.Thr10Ser
XM_005260517.1:c.28A>T XP_005260574.1:p.Thr10Ser
XM_011529007.1:c.28A>T XP_011527309.1:p.Thr10Ser
XM_011529008.1:c.28A>T XP_011527310.1:p.Thr10Ser
XR_936612.1:n.261A>T
NM_003098.3:c.28A>T MANE Select NP_003089.1:p.Thr10Ser