Canonical Allele Identifier: CA393055940

Gene: GRAMD2A

Linked Data

• MyVariant Identifiers: chr15:g.72462257G>C (hg19) ; chr15:g.72169916G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72169916G>C , CM000677.2:g.72169916G>C	GRCh38
NC_000015.9:g.72462257G>C , CM000677.1:g.72462257G>C	GRCh37
NC_000015.8:g.70249311G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000309731.12:c.65C>G MANE Select	ENSP00000311657.7:p.Thr22Arg
ENST00000309731.11:c.65C>G	ENSP00000311657.7:p.Thr22Arg
ENST00000562288.1:c.29C>G	ENSP00000457155.1:p.Thr10Arg
ENST00000563133.5:n.220C>G
ENST00000564129.5:c.35C>G	ENSP00000457660.1:p.Thr12Arg
ENST00000568594.5:c.44C>G	ENSP00000457383.1:p.Thr15Arg
ENST00000570275.5:c.29C>G	ENSP00000457088.1:p.Thr10Arg
NM_001012642.2:c.65C>G	NP_001012660.1:p.Thr22Arg
XM_011521327.1:c.62C>G	XP_011519629.1:p.Thr21Arg
XM_011521328.1:c.59C>G	XP_011519630.1:p.Thr20Arg
XM_011521329.1:c.35C>G	XP_011519631.1:p.Thr12Arg
XM_011521330.1:c.29C>G	XP_011519632.1:p.Thr10Arg
XM_011521331.1:c.65C>G	XP_011519633.1:p.Thr22Arg
XM_011521332.1:c.-191C>G	XP_011519634.1:n.-191C>G
XM_011521333.1:c.-191C>G	XP_011519635.1:n.-191C>G
XM_011521327.2:c.62C>G	XP_011519629.1:p.Thr21Arg
XM_011521328.3:c.59C>G	XP_011519630.1:p.Thr20Arg
XM_011521329.2:c.35C>G	XP_011519631.1:p.Thr12Arg
XM_011521330.2:c.29C>G	XP_011519632.1:p.Thr10Arg
XM_011521331.2:c.65C>G	XP_011519633.1:p.Thr22Arg
XM_011521332.3:c.-191C>G	XP_011519634.1:n.-191C>G
XM_011521333.3:c.-191C>G	XP_011519635.1:n.-191C>G
XM_017021997.1:c.-175C>G	XP_016877486.1:n.-175C>G
XM_017021998.1:c.-175C>G	XP_016877487.1:n.-175C>G
XM_024449868.1:c.14C>G	XP_024305636.1:p.Thr5Arg
NM_001012642.3:c.65C>G MANE Select	NP_001012660.1:p.Thr22Arg