Canonical Allele Identifier: CA393055992

Gene: GRAMD2A

Linked Data

• MyVariant Identifiers: chr15:g.72462265G>T (hg19) ; chr15:g.72169924G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72169924G>T , CM000677.2:g.72169924G>T	GRCh38
NC_000015.9:g.72462265G>T , CM000677.1:g.72462265G>T	GRCh37
NC_000015.8:g.70249319G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000309731.12:c.57C>A MANE Select	ENSP00000311657.7:p.His19Gln
ENST00000309731.11:c.57C>A	ENSP00000311657.7:p.His19Gln
ENST00000562288.1:c.21C>A	ENSP00000457155.1:p.His7Gln
ENST00000563133.5:n.212C>A
ENST00000564129.5:c.27C>A	ENSP00000457660.1:p.His9Gln
ENST00000568594.5:c.36C>A	ENSP00000457383.1:p.His12Gln
ENST00000570275.5:c.21C>A	ENSP00000457088.1:p.His7Gln
NM_001012642.2:c.57C>A	NP_001012660.1:p.His19Gln
XM_011521327.1:c.54C>A	XP_011519629.1:p.His18Gln
XM_011521328.1:c.51C>A	XP_011519630.1:p.His17Gln
XM_011521329.1:c.27C>A	XP_011519631.1:p.His9Gln
XM_011521330.1:c.21C>A	XP_011519632.1:p.His7Gln
XM_011521331.1:c.57C>A	XP_011519633.1:p.His19Gln
XM_011521332.1:c.-199C>A	XP_011519634.1:n.-199C>A
XM_011521333.1:c.-199C>A	XP_011519635.1:n.-199C>A
XM_011521327.2:c.54C>A	XP_011519629.1:p.His18Gln
XM_011521328.3:c.51C>A	XP_011519630.1:p.His17Gln
XM_011521329.2:c.27C>A	XP_011519631.1:p.His9Gln
XM_011521330.2:c.21C>A	XP_011519632.1:p.His7Gln
XM_011521331.2:c.57C>A	XP_011519633.1:p.His19Gln
XM_011521332.3:c.-199C>A	XP_011519634.1:n.-199C>A
XM_011521333.3:c.-199C>A	XP_011519635.1:n.-199C>A
XM_017021997.1:c.-183C>A	XP_016877486.1:n.-183C>A
XM_017021998.1:c.-183C>A	XP_016877487.1:n.-183C>A
XM_024449868.1:c.6C>A	XP_024305636.1:p.His2Gln
NM_001012642.3:c.57C>A MANE Select	NP_001012660.1:p.His19Gln