Canonical Allele Identifier: CA2186665686

Gene: GRAMD2A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72169928A= , CM000677.2:g.72169928A=	GRCh38
NC_000015.9:g.72462269A= , CM000677.1:g.72462269A=	GRCh37
NC_000015.8:g.70249323A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000309731.12:c.53T= MANE Select	ENSP00000311657.7:p.Met18=
ENST00000309731.11:c.53T=	ENSP00000311657.7:p.Met18=
ENST00000562288.1:c.17T=	ENSP00000457155.1:p.Met6=
ENST00000563133.5:n.208T=
ENST00000564129.5:c.23T=	ENSP00000457660.1:p.Met8=
ENST00000568594.5:c.32T=	ENSP00000457383.1:p.Met11=
ENST00000570275.5:c.17T=	ENSP00000457088.1:p.Met6=
NM_001012642.2:c.53T=	NP_001012660.1:p.Met18=
XM_011521327.1:c.50T=	XP_011519629.1:p.Met17=
XM_011521328.1:c.47T=	XP_011519630.1:p.Met16=
XM_011521329.1:c.23T=	XP_011519631.1:p.Met8=
XM_011521330.1:c.17T=	XP_011519632.1:p.Met6=
XM_011521331.1:c.53T=	XP_011519633.1:p.Met18=
XM_011521332.1:c.-203T=	XP_011519634.1:n.-203T=
XM_011521333.1:c.-203T=	XP_011519635.1:n.-203T=
XM_011521327.2:c.50T=	XP_011519629.1:p.Met17=
XM_011521328.3:c.47T=	XP_011519630.1:p.Met16=
XM_011521329.2:c.23T=	XP_011519631.1:p.Met8=
XM_011521330.2:c.17T=	XP_011519632.1:p.Met6=
XM_011521331.2:c.53T=	XP_011519633.1:p.Met18=
XM_011521332.3:c.-203T=	XP_011519634.1:n.-203T=
XM_011521333.3:c.-203T=	XP_011519635.1:n.-203T=
XM_017021997.1:c.-187T=	XP_016877486.1:n.-187T=
XM_017021998.1:c.-187T=	XP_016877487.1:n.-187T=
XM_024449868.1:c.2T=	XP_024305636.1:p.Met1=
NM_001012642.3:c.53T= MANE Select	NP_001012660.1:p.Met18=