Canonical Allele Identifier: CA2360753104

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438971T= , CM000682.2:g.33438971T=	GRCh38
NC_000020.10:g.32026777T= , CM000682.1:g.32026777T=	GRCh37
NC_000020.9:g.31490438T=	NCBI36
NG_011622.1:g.9922A= , LRG_332:g.9922A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.366A= MANE Select	ENSP00000217381.2:p.Ala122=
ENST00000217381.2:c.366A=	ENSP00000217381.2:p.Ala122=
NM_003098.2:c.366A= , LRG_332t1:c.366A=	NP_003089.1:p.Ala122=
XM_005260517.1:c.366A=	XP_005260574.1:p.Ala122=
XM_011529007.1:c.366A=	XP_011527309.1:p.Ala122=
XM_011529008.1:c.366A=	XP_011527310.1:p.Ala122=
XR_936612.1:n.599A=
XM_024451971.1:c.39A=	XP_024307739.1:p.Ala13=
NM_003098.3:c.366A= MANE Select	NP_003089.1:p.Ala122=