Canonical Allele Identifier: CA1806383442

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101558674A= , CM000670.2:g.101558674A=	GRCh38
NC_000008.10:g.102570902A= , CM000670.1:g.102570902A=	GRCh37
NC_000008.9:g.102640078A=	NCBI36
NG_011971.1:g.71235A=
NG_011971.2:g.71235A=

Transcript Alleles

HGVS	Amino-acid Change
NM_024915.4:c.540A= MANE Select	NP_079191.2:p.Glu180=
ENST00000646743.1:c.540A= MANE Select	ENSP00000495564.1:p.Glu180=
NM_001330593.1:c.492A=	NP_001317522.1:p.Glu164=
NM_001330593.2:c.492A=	NP_001317522.1:p.Glu164=
NM_024915.3:c.540A=	NP_079191.2:p.Glu180=
ENST00000251808.7:c.540A=	ENSP00000251808.3:p.Glu180=
ENST00000395927.1:c.492A=	ENSP00000379260.1:p.Glu164=
XM_011517305.1:c.492A=	XP_011515607.1:p.Glu164=
XM_011517306.1:c.492A=	XP_011515608.1:p.Glu164=
XM_011517306.3:c.492A=	XP_011515608.1:p.Glu164=
XM_011517307.1:c.540A=	XP_011515609.1:p.Glu180=
XM_011517307.3:c.540A=	XP_011515609.1:p.Glu180=