Canonical Allele Identifier: CA1806416463

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101632325T= , CM000670.2:g.101632325T=	GRCh38
NC_000008.10:g.102644553T= , CM000670.1:g.102644553T=	GRCh37
NC_000008.9:g.102713729T=	NCBI36
NG_011971.1:g.144886T=
NG_011971.2:g.144886T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.1445T= MANE Select	ENSP00000495564.1:p.Ile482=
ENST00000251808.7:c.1445T=	ENSP00000251808.3:p.Ile482=
ENST00000395927.1:c.1397T=	ENSP00000379260.1:p.Ile466=
ENST00000517674.5:n.100T=
NM_024915.3:c.1445T=	NP_079191.2:p.Ile482=
XM_011517305.1:c.1397T=	XP_011515607.1:p.Ile466=
XM_011517306.1:c.1397T=	XP_011515608.1:p.Ile466=
XM_011517307.1:c.1445T=	XP_011515609.1:p.Ile482=
NM_001330593.1:c.1397T=	NP_001317522.1:p.Ile466=
XM_011517306.3:c.1397T=	XP_011515608.1:p.Ile466=
XM_011517307.3:c.1445T=	XP_011515609.1:p.Ile482=
NM_001330593.2:c.1397T=	NP_001317522.1:p.Ile466=
NM_024915.4:c.1445T= MANE Select	NP_079191.2:p.Ile482=