Canonical Allele Identifier: CA1806376432

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101543415C= , CM000670.2:g.101543415C=	GRCh38
NC_000008.10:g.102555643C= , CM000670.1:g.102555643C=	GRCh37
NC_000008.9:g.102624819C=	NCBI36
NG_011971.1:g.55976C=
NG_011971.2:g.55976C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.195C= MANE Select	ENSP00000495564.1:p.Gly65=
ENST00000251808.7:c.195C=	ENSP00000251808.3:p.Gly65=
ENST00000395927.1:c.147C=	ENSP00000379260.1:p.Gly49=
ENST00000472106.2:n.523C=
NM_024915.3:c.195C=	NP_079191.2:p.Gly65=
XM_011517305.1:c.147C=	XP_011515607.1:p.Gly49=
XM_011517306.1:c.147C=	XP_011515608.1:p.Gly49=
XM_011517307.1:c.195C=	XP_011515609.1:p.Gly65=
NM_001330593.1:c.147C=	NP_001317522.1:p.Gly49=
XM_011517306.3:c.147C=	XP_011515608.1:p.Gly49=
XM_011517307.3:c.195C=	XP_011515609.1:p.Gly65=
NM_001330593.2:c.147C=	NP_001317522.1:p.Gly49=
NM_024915.4:c.195C= MANE Select	NP_079191.2:p.Gly65=