Canonical Allele Identifier: CA1806376408

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101543296C= , CM000670.2:g.101543296C=	GRCh38
NC_000008.10:g.102555524C= , CM000670.1:g.102555524C=	GRCh37
NC_000008.9:g.102624700C=	NCBI36
NG_011971.1:g.55857C=
NG_011971.2:g.55857C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.76C= MANE Select	ENSP00000495564.1:p.Arg26=
ENST00000251808.7:c.76C=	ENSP00000251808.3:p.Arg26=
ENST00000395927.1:c.28C=	ENSP00000379260.1:p.Arg10=
ENST00000472106.2:n.404C=
NM_024915.3:c.76C=	NP_079191.2:p.Arg26=
XM_011517305.1:c.28C=	XP_011515607.1:p.Arg10=
XM_011517306.1:c.28C=	XP_011515608.1:p.Arg10=
XM_011517307.1:c.76C=	XP_011515609.1:p.Arg26=
NM_001330593.1:c.28C=	NP_001317522.1:p.Arg10=
XM_011517306.3:c.28C=	XP_011515608.1:p.Arg10=
XM_011517307.3:c.76C=	XP_011515609.1:p.Arg26=
NM_001330593.2:c.28C=	NP_001317522.1:p.Arg10=
NM_024915.4:c.76C= MANE Select	NP_079191.2:p.Arg26=