Canonical Allele Identifier: CA393055957

Gene: GRAMD2A

Linked Data

• MyVariant Identifiers: chr15:g.72462259C>A (hg19) ; chr15:g.72169918C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72169918C>A , CM000677.2:g.72169918C>A	GRCh38
NC_000015.9:g.72462259C>A , CM000677.1:g.72462259C>A	GRCh37
NC_000015.8:g.70249313C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000309731.12:c.63G>T MANE Select	ENSP00000311657.7:p.Lys21Asn
ENST00000309731.11:c.63G>T	ENSP00000311657.7:p.Lys21Asn
ENST00000562288.1:c.27G>T	ENSP00000457155.1:p.Lys9Asn
ENST00000563133.5:n.218G>T
ENST00000564129.5:c.33G>T	ENSP00000457660.1:p.Lys11Asn
ENST00000568594.5:c.42G>T	ENSP00000457383.1:p.Lys14Asn
ENST00000570275.5:c.27G>T	ENSP00000457088.1:p.Lys9Asn
NM_001012642.2:c.63G>T	NP_001012660.1:p.Lys21Asn
XM_011521327.1:c.60G>T	XP_011519629.1:p.Lys20Asn
XM_011521328.1:c.57G>T	XP_011519630.1:p.Lys19Asn
XM_011521329.1:c.33G>T	XP_011519631.1:p.Lys11Asn
XM_011521330.1:c.27G>T	XP_011519632.1:p.Lys9Asn
XM_011521331.1:c.63G>T	XP_011519633.1:p.Lys21Asn
XM_011521332.1:c.-193G>T	XP_011519634.1:n.-193G>T
XM_011521333.1:c.-193G>T	XP_011519635.1:n.-193G>T
XM_011521327.2:c.60G>T	XP_011519629.1:p.Lys20Asn
XM_011521328.3:c.57G>T	XP_011519630.1:p.Lys19Asn
XM_011521329.2:c.33G>T	XP_011519631.1:p.Lys11Asn
XM_011521330.2:c.27G>T	XP_011519632.1:p.Lys9Asn
XM_011521331.2:c.63G>T	XP_011519633.1:p.Lys21Asn
XM_011521332.3:c.-193G>T	XP_011519634.1:n.-193G>T
XM_011521333.3:c.-193G>T	XP_011519635.1:n.-193G>T
XM_017021997.1:c.-177G>T	XP_016877486.1:n.-177G>T
XM_017021998.1:c.-177G>T	XP_016877487.1:n.-177G>T
XM_024449868.1:c.12G>T	XP_024305636.1:p.Lys4Asn
NM_001012642.3:c.63G>T MANE Select	NP_001012660.1:p.Lys21Asn