Canonical Allele Identifier: CA2360753093

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438938A= , CM000682.2:g.33438938A=	GRCh38
NC_000020.10:g.32026744A= , CM000682.1:g.32026744A=	GRCh37
NC_000020.9:g.31490405A=	NCBI36
NG_011622.1:g.9955T= , LRG_332:g.9955T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.399T= MANE Select	ENSP00000217381.2:p.Asp133=
ENST00000217381.2:c.399T=	ENSP00000217381.2:p.Asp133=
NM_003098.2:c.399T= , LRG_332t1:c.399T=	NP_003089.1:p.Asp133=
XM_005260517.1:c.399T=	XP_005260574.1:p.Asp133=
XM_011529007.1:c.399T=	XP_011527309.1:p.Asp133=
XM_011529008.1:c.399T=	XP_011527310.1:p.Asp133=
XR_936612.1:n.632T=
XM_024451971.1:c.72T=	XP_024307739.1:p.Asp24=
NM_003098.3:c.399T= MANE Select	NP_003089.1:p.Asp133=