Canonical Allele Identifier: CA4830438

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101577503G>A , CM000670.2:g.101577503G>A	GRCh38
NC_000008.10:g.102589731G>A , CM000670.1:g.102589731G>A	GRCh37
NC_000008.9:g.102658907G>A	NCBI36
NG_011971.1:g.90064G>A
NG_011971.2:g.90064G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.987G>A MANE Select	ENSP00000495564.1:p.Gln329=
ENST00000251808.7:c.987G>A	ENSP00000251808.3:p.Gln329=
ENST00000395927.1:c.939G>A	ENSP00000379260.1:p.Gln313=
NM_024915.3:c.987G>A	NP_079191.2:p.Gln329=
XM_011517305.1:c.939G>A	XP_011515607.1:p.Gln313=
XM_011517306.1:c.939G>A	XP_011515608.1:p.Gln313=
XM_011517307.1:c.987G>A	XP_011515609.1:p.Gln329=
NM_001330593.1:c.939G>A	NP_001317522.1:p.Gln313=
XM_011517306.3:c.939G>A	XP_011515608.1:p.Gln313=
XM_011517307.3:c.987G>A	XP_011515609.1:p.Gln329=
NM_001330593.2:c.939G>A	NP_001317522.1:p.Gln313=
NM_024915.4:c.987G>A MANE Select	NP_079191.2:p.Gln329=