Canonical Allele Identifier: CA393055968

Gene: GRAMD2A

Linked Data

• MyVariant Identifiers: chr15:g.72462261T>G (hg19) ; chr15:g.72169920T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72169920T>G , CM000677.2:g.72169920T>G	GRCh38
NC_000015.9:g.72462261T>G , CM000677.1:g.72462261T>G	GRCh37
NC_000015.8:g.70249315T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000309731.12:c.61A>C MANE Select	ENSP00000311657.7:p.Lys21Gln
ENST00000309731.11:c.61A>C	ENSP00000311657.7:p.Lys21Gln
ENST00000562288.1:c.25A>C	ENSP00000457155.1:p.Lys9Gln
ENST00000563133.5:n.216A>C
ENST00000564129.5:c.31A>C	ENSP00000457660.1:p.Lys11Gln
ENST00000568594.5:c.40A>C	ENSP00000457383.1:p.Lys14Gln
ENST00000570275.5:c.25A>C	ENSP00000457088.1:p.Lys9Gln
NM_001012642.2:c.61A>C	NP_001012660.1:p.Lys21Gln
XM_011521327.1:c.58A>C	XP_011519629.1:p.Lys20Gln
XM_011521328.1:c.55A>C	XP_011519630.1:p.Lys19Gln
XM_011521329.1:c.31A>C	XP_011519631.1:p.Lys11Gln
XM_011521330.1:c.25A>C	XP_011519632.1:p.Lys9Gln
XM_011521331.1:c.61A>C	XP_011519633.1:p.Lys21Gln
XM_011521332.1:c.-195A>C	XP_011519634.1:n.-195A>C
XM_011521333.1:c.-195A>C	XP_011519635.1:n.-195A>C
XM_011521327.2:c.58A>C	XP_011519629.1:p.Lys20Gln
XM_011521328.3:c.55A>C	XP_011519630.1:p.Lys19Gln
XM_011521329.2:c.31A>C	XP_011519631.1:p.Lys11Gln
XM_011521330.2:c.25A>C	XP_011519632.1:p.Lys9Gln
XM_011521331.2:c.61A>C	XP_011519633.1:p.Lys21Gln
XM_011521332.3:c.-195A>C	XP_011519634.1:n.-195A>C
XM_011521333.3:c.-195A>C	XP_011519635.1:n.-195A>C
XM_017021997.1:c.-179A>C	XP_016877486.1:n.-179A>C
XM_017021998.1:c.-179A>C	XP_016877487.1:n.-179A>C
XM_024449868.1:c.10A>C	XP_024305636.1:p.Lys4Gln
NM_001012642.3:c.61A>C MANE Select	NP_001012660.1:p.Lys21Gln