Canonical Allele Identifier: CA3164258751

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101558678C= , CM000670.2:g.101558678C=	GRCh38
NC_000008.10:g.102570906C= , CM000670.1:g.102570906C=	GRCh37
NC_000008.9:g.102640082C=	NCBI36
NG_011971.1:g.71239C=
NG_011971.2:g.71239C=

Transcript Alleles

HGVS	Amino-acid Change
NM_024915.4:c.544C= MANE Select	NP_079191.2:p.Gln182=
ENST00000646743.1:c.544C= MANE Select	ENSP00000495564.1:p.Gln182=
NM_001330593.1:c.496C=	NP_001317522.1:p.Gln166=
NM_001330593.2:c.496C=	NP_001317522.1:p.Gln166=
NM_024915.3:c.544C=	NP_079191.2:p.Gln182=
ENST00000251808.7:c.544C=	ENSP00000251808.3:p.Gln182=
ENST00000395927.1:c.496C=	ENSP00000379260.1:p.Gln166=
XM_011517305.1:c.496C=	XP_011515607.1:p.Gln166=
XM_011517306.1:c.496C=	XP_011515608.1:p.Gln166=
XM_011517306.3:c.496C=	XP_011515608.1:p.Gln166=
XM_011517307.1:c.544C=	XP_011515609.1:p.Gln182=
XM_011517307.3:c.544C=	XP_011515609.1:p.Gln182=