Canonical Allele Identifier: CA1806383443

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101558677G= , CM000670.2:g.101558677G=	GRCh38
NC_000008.10:g.102570905G= , CM000670.1:g.102570905G=	GRCh37
NC_000008.9:g.102640081G=	NCBI36
NG_011971.1:g.71238G=
NG_011971.2:g.71238G=

Transcript Alleles

HGVS	Amino-acid Change
NM_024915.4:c.543G= MANE Select	NP_079191.2:p.Glu181=
ENST00000646743.1:c.543G= MANE Select	ENSP00000495564.1:p.Glu181=
NM_001330593.1:c.495G=	NP_001317522.1:p.Glu165=
NM_001330593.2:c.495G=	NP_001317522.1:p.Glu165=
NM_024915.3:c.543G=	NP_079191.2:p.Glu181=
ENST00000251808.7:c.543G=	ENSP00000251808.3:p.Glu181=
ENST00000395927.1:c.495G=	ENSP00000379260.1:p.Glu165=
XM_011517305.1:c.495G=	XP_011515607.1:p.Glu165=
XM_011517306.1:c.495G=	XP_011515608.1:p.Glu165=
XM_011517306.3:c.495G=	XP_011515608.1:p.Glu165=
XM_011517307.1:c.543G=	XP_011515609.1:p.Glu181=
XM_011517307.3:c.543G=	XP_011515609.1:p.Glu181=