Canonical Allele Identifier: CA1806433112

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101667681G= , CM000670.2:g.101667681G=	GRCh38
NC_000008.10:g.102679909G= , CM000670.1:g.102679909G=	GRCh37
NC_000008.9:g.102749085G=	NCBI36
NG_011971.1:g.180242G=
NG_011971.2:g.180242G=

Transcript Alleles

HGVS	Amino-acid Change
NM_024915.4:c.*978G= MANE Select	NP_079191.2:n.*978G=
ENST00000646743.1:c.*978G= MANE Select	ENSP00000495564.1:n.*978G=
NM_001330593.1:c.*978G=	NP_001317522.1:n.*978G=
NM_001330593.2:c.*978G=	NP_001317522.1:n.*978G=
NM_024915.3:c.*978G=	NP_079191.2:n.*978G=
ENST00000251808.7:c.*978G=	ENSP00000251808.3:n.*978G=
XM_011517305.1:c.*978G=	XP_011515607.1:n.*978G=
XM_011517306.1:c.*978G=	XP_011515608.1:n.*978G=
XM_011517306.3:c.*978G=	XP_011515608.1:n.*978G=
XM_011517307.1:c.1763+3163G=	XP_011515609.1:n.1763+3163G=
XM_011517307.3:c.1763+3163G=	XP_011515609.1:n.1763+3163G=