Canonical Allele Identifier: CA393055994

Gene: GRAMD2A

Linked Data

• MyVariant Identifiers: chr15:g.72462266T>C (hg19) ; chr15:g.72169925T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72169925T>C , CM000677.2:g.72169925T>C	GRCh38
NC_000015.9:g.72462266T>C , CM000677.1:g.72462266T>C	GRCh37
NC_000015.8:g.70249320T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000309731.12:c.56A>G MANE Select	ENSP00000311657.7:p.His19Arg
ENST00000309731.11:c.56A>G	ENSP00000311657.7:p.His19Arg
ENST00000562288.1:c.20A>G	ENSP00000457155.1:p.His7Arg
ENST00000563133.5:n.211A>G
ENST00000564129.5:c.26A>G	ENSP00000457660.1:p.His9Arg
ENST00000568594.5:c.35A>G	ENSP00000457383.1:p.His12Arg
ENST00000570275.5:c.20A>G	ENSP00000457088.1:p.His7Arg
NM_001012642.2:c.56A>G	NP_001012660.1:p.His19Arg
XM_011521327.1:c.53A>G	XP_011519629.1:p.His18Arg
XM_011521328.1:c.50A>G	XP_011519630.1:p.His17Arg
XM_011521329.1:c.26A>G	XP_011519631.1:p.His9Arg
XM_011521330.1:c.20A>G	XP_011519632.1:p.His7Arg
XM_011521331.1:c.56A>G	XP_011519633.1:p.His19Arg
XM_011521332.1:c.-200A>G	XP_011519634.1:n.-200A>G
XM_011521333.1:c.-200A>G	XP_011519635.1:n.-200A>G
XM_011521327.2:c.53A>G	XP_011519629.1:p.His18Arg
XM_011521328.3:c.50A>G	XP_011519630.1:p.His17Arg
XM_011521329.2:c.26A>G	XP_011519631.1:p.His9Arg
XM_011521330.2:c.20A>G	XP_011519632.1:p.His7Arg
XM_011521331.2:c.56A>G	XP_011519633.1:p.His19Arg
XM_011521332.3:c.-200A>G	XP_011519634.1:n.-200A>G
XM_011521333.3:c.-200A>G	XP_011519635.1:n.-200A>G
XM_017021997.1:c.-184A>G	XP_016877486.1:n.-184A>G
XM_017021998.1:c.-184A>G	XP_016877487.1:n.-184A>G
XM_024449868.1:c.5A>G	XP_024305636.1:p.His2Arg
NM_001012642.3:c.56A>G MANE Select	NP_001012660.1:p.His19Arg