Canonical Allele Identifier: CA2360740169

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33408744G= , CM000682.2:g.33408744G=	GRCh38
NC_000020.10:g.31996550G= , CM000682.1:g.31996550G=	GRCh37
NC_000020.9:g.31460211G=	NCBI36
NG_011622.1:g.40149C= , LRG_332:g.40149C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.1382C= MANE Select	ENSP00000217381.2:p.Ala461=
ENST00000217381.2:c.1382C=	ENSP00000217381.2:p.Ala461=
NM_003098.2:c.1382C= , LRG_332t1:c.1382C=	NP_003089.1:p.Ala461=
XM_005260517.1:c.1382C=	XP_005260574.1:p.Ala461=
XM_011529007.1:c.1414C=	XP_011527309.1:p.Pro472=
XM_011529008.1:c.1414C=	XP_011527310.1:p.Pro472=
XR_936612.1:n.1418C=
XM_024451971.1:c.1055C=	XP_024307739.1:p.Ala352=
NM_003098.3:c.1382C= MANE Select	NP_003089.1:p.Ala461=