Canonical Allele Identifier: CA2360753073

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438879T= , CM000682.2:g.33438879T=	GRCh38
NC_000020.10:g.32026685T= , CM000682.1:g.32026685T=	GRCh37
NC_000020.9:g.31490346T=	NCBI36
NG_011622.1:g.10014A= , LRG_332:g.10014A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.458A= MANE Select	ENSP00000217381.2:p.Gln153=
ENST00000217381.2:c.458A=	ENSP00000217381.2:p.Gln153=
NM_003098.2:c.458A= , LRG_332t1:c.458A=	NP_003089.1:p.Gln153=
XM_005260517.1:c.458A=	XP_005260574.1:p.Gln153=
XM_011529007.1:c.458A=	XP_011527309.1:p.Gln153=
XM_011529008.1:c.458A=	XP_011527310.1:p.Gln153=
XR_936612.1:n.691A=
XM_024451971.1:c.131A=	XP_024307739.1:p.Gln44=
NM_003098.3:c.458A= MANE Select	NP_003089.1:p.Gln153=