Canonical Allele Identifier: CA2360752949

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438566T= , CM000682.2:g.33438566T=	GRCh38
NC_000020.10:g.32026372T= , CM000682.1:g.32026372T=	GRCh37
NC_000020.9:g.31490033T=	NCBI36
NG_011622.1:g.10327A= , LRG_332:g.10327A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+275A= MANE Select	ENSP00000217381.2:n.496+275A=
ENST00000217381.2:c.496+275A=	ENSP00000217381.2:n.496+275A=
NM_003098.2:c.496+275A= , LRG_332t1:c.496+275A=	NP_003089.1:n.496+275A=
XM_005260517.1:c.496+275A=	XP_005260574.1:n.496+275A=
XM_011529007.1:c.496+275A=	XP_011527309.1:n.496+275A=
XM_011529008.1:c.496+275A=	XP_011527310.1:n.496+275A=
XR_936612.1:n.729+275A=
XM_024451971.1:c.169+275A=	XP_024307739.1:n.169+275A=
NM_003098.3:c.496+275A= MANE Select	NP_003089.1:n.496+275A=