Canonical Allele Identifier: CA2360755008

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443564C= , CM000682.2:g.33443564C=	GRCh38
NC_000020.10:g.32031370C= , CM000682.1:g.32031370C=	GRCh37
NC_000020.9:g.31495031C=	NCBI36
NG_011622.1:g.5329G= , LRG_332:g.5329G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.57G= MANE Select	ENSP00000217381.2:p.Ala19=
ENST00000217381.2:c.57G=	ENSP00000217381.2:p.Ala19=
NM_003098.2:c.57G= , LRG_332t1:c.57G=	NP_003089.1:p.Ala19=
XM_005260517.1:c.57G=	XP_005260574.1:p.Ala19=
XM_011529007.1:c.57G=	XP_011527309.1:p.Ala19=
XM_011529008.1:c.57G=	XP_011527310.1:p.Ala19=
XR_936612.1:n.290G=
NM_003098.3:c.57G= MANE Select	NP_003089.1:p.Ala19=