Canonical Allele Identifier: CA2360755005

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443559G= , CM000682.2:g.33443559G=	GRCh38
NC_000020.10:g.32031365G= , CM000682.1:g.32031365G=	GRCh37
NC_000020.9:g.31495026G=	NCBI36
NG_011622.1:g.5334C= , LRG_332:g.5334C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.62C= MANE Select	ENSP00000217381.2:p.Ser21=
ENST00000217381.2:c.62C=	ENSP00000217381.2:p.Ser21=
NM_003098.2:c.62C= , LRG_332t1:c.62C=	NP_003089.1:p.Ser21=
XM_005260517.1:c.62C=	XP_005260574.1:p.Ser21=
XM_011529007.1:c.62C=	XP_011527309.1:p.Ser21=
XM_011529008.1:c.62C=	XP_011527310.1:p.Ser21=
XR_936612.1:n.295C=
NM_003098.3:c.62C= MANE Select	NP_003089.1:p.Ser21=