Canonical Allele Identifier: CA491132877

Gene: GRAMD2A

Linked Data

• MyVariant Identifiers: chr15:g.72462262T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72169921T>C , CM000677.2:g.72169921T>C	GRCh38
NC_000015.9:g.72462262T>C , CM000677.1:g.72462262T>C	GRCh37
NC_000015.8:g.70249316T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000309731.12:c.60A>G MANE Select	ENSP00000311657.7:p.Arg20=
ENST00000309731.11:c.60A>G	ENSP00000311657.7:p.Arg20=
ENST00000562288.1:c.24A>G	ENSP00000457155.1:p.Arg8=
ENST00000563133.5:n.215A>G
ENST00000564129.5:c.30A>G	ENSP00000457660.1:p.Arg10=
ENST00000568594.5:c.39A>G	ENSP00000457383.1:p.Arg13=
ENST00000570275.5:c.24A>G	ENSP00000457088.1:p.Arg8=
NM_001012642.2:c.60A>G	NP_001012660.1:p.Arg20=
XM_011521327.1:c.57A>G	XP_011519629.1:p.Arg19=
XM_011521328.1:c.54A>G	XP_011519630.1:p.Arg18=
XM_011521329.1:c.30A>G	XP_011519631.1:p.Arg10=
XM_011521330.1:c.24A>G	XP_011519632.1:p.Arg8=
XM_011521331.1:c.60A>G	XP_011519633.1:p.Arg20=
XM_011521332.1:c.-196A>G	XP_011519634.1:n.-196A>G
XM_011521333.1:c.-196A>G	XP_011519635.1:n.-196A>G
XM_011521327.2:c.57A>G	XP_011519629.1:p.Arg19=
XM_011521328.3:c.54A>G	XP_011519630.1:p.Arg18=
XM_011521329.2:c.30A>G	XP_011519631.1:p.Arg10=
XM_011521330.2:c.24A>G	XP_011519632.1:p.Arg8=
XM_011521331.2:c.60A>G	XP_011519633.1:p.Arg20=
XM_011521332.3:c.-196A>G	XP_011519634.1:n.-196A>G
XM_011521333.3:c.-196A>G	XP_011519635.1:n.-196A>G
XM_017021997.1:c.-180A>G	XP_016877486.1:n.-180A>G
XM_017021998.1:c.-180A>G	XP_016877487.1:n.-180A>G
XM_024449868.1:c.9A>G	XP_024305636.1:p.Arg3=
NM_001012642.3:c.60A>G MANE Select	NP_001012660.1:p.Arg20=