Canonical Allele Identifier: CA2186665680

Gene: GRAMD2A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72169914C= , CM000677.2:g.72169914C=	GRCh38
NC_000015.9:g.72462255C= , CM000677.1:g.72462255C=	GRCh37
NC_000015.8:g.70249309C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001012642.3:c.67G= MANE Select	NP_001012660.1:p.Ala23=
ENST00000309731.12:c.67G= MANE Select	ENSP00000311657.7:p.Ala23=
NM_001012642.2:c.67G=	NP_001012660.1:p.Ala23=
ENST00000309731.11:c.67G=	ENSP00000311657.7:p.Ala23=
ENST00000562288.1:c.31G=	ENSP00000457155.1:p.Ala11=
ENST00000563133.5:n.222G=
ENST00000564129.5:c.37G=	ENSP00000457660.1:p.Ala13=
ENST00000568594.5:c.46G=	ENSP00000457383.1:p.Ala16=
ENST00000570275.5:c.31G=	ENSP00000457088.1:p.Ala11=
XM_011521327.1:c.64G=	XP_011519629.1:p.Ala22=
XM_011521327.2:c.64G=	XP_011519629.1:p.Ala22=
XM_011521328.1:c.61G=	XP_011519630.1:p.Ala21=
XM_011521328.3:c.61G=	XP_011519630.1:p.Ala21=
XM_011521329.1:c.37G=	XP_011519631.1:p.Ala13=
XM_011521329.2:c.37G=	XP_011519631.1:p.Ala13=
XM_011521330.1:c.31G=	XP_011519632.1:p.Ala11=
XM_011521330.2:c.31G=	XP_011519632.1:p.Ala11=
XM_011521331.1:c.67G=	XP_011519633.1:p.Ala23=
XM_011521331.2:c.67G=	XP_011519633.1:p.Ala23=
XM_011521332.1:c.-189G=	XP_011519634.1:n.-189G=
XM_011521332.3:c.-189G=	XP_011519634.1:n.-189G=
XM_011521333.1:c.-189G=	XP_011519635.1:n.-189G=
XM_011521333.3:c.-189G=	XP_011519635.1:n.-189G=
XM_017021997.1:c.-173G=	XP_016877486.1:n.-173G=
XM_017021998.1:c.-173G=	XP_016877487.1:n.-173G=
XM_024449868.1:c.16G=	XP_024305636.1:p.Ala6=