Canonical Allele Identifier: CA2360755029

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443601G= , CM000682.2:g.33443601G=	GRCh38
NC_000020.10:g.32031407G= , CM000682.1:g.32031407G=	GRCh37
NC_000020.9:g.31495068G=	NCBI36
NG_011622.1:g.5292C= , LRG_332:g.5292C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.20C= MANE Select	ENSP00000217381.2:p.Ala7=
ENST00000217381.2:c.20C=	ENSP00000217381.2:p.Ala7=
NM_003098.2:c.20C= , LRG_332t1:c.20C=	NP_003089.1:p.Ala7=
XM_005260517.1:c.20C=	XP_005260574.1:p.Ala7=
XM_011529007.1:c.20C=	XP_011527309.1:p.Ala7=
XM_011529008.1:c.20C=	XP_011527310.1:p.Ala7=
XR_936612.1:n.253C=
NM_003098.3:c.20C= MANE Select	NP_003089.1:p.Ala7=