Canonical Allele Identifier: CA2360753107

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438978C= , CM000682.2:g.33438978C=	GRCh38
NC_000020.10:g.32026784C= , CM000682.1:g.32026784C=	GRCh37
NC_000020.9:g.31490445C=	NCBI36
NG_011622.1:g.9915G= , LRG_332:g.9915G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.359G= MANE Select	ENSP00000217381.2:p.Gly120=
ENST00000217381.2:c.359G=	ENSP00000217381.2:p.Gly120=
NM_003098.2:c.359G= , LRG_332t1:c.359G=	NP_003089.1:p.Gly120=
XM_005260517.1:c.359G=	XP_005260574.1:p.Gly120=
XM_011529007.1:c.359G=	XP_011527309.1:p.Gly120=
XM_011529008.1:c.359G=	XP_011527310.1:p.Gly120=
XR_936612.1:n.592G=
XM_024451971.1:c.32G=	XP_024307739.1:p.Gly11=
NM_003098.3:c.359G= MANE Select	NP_003089.1:p.Gly120=