Canonical Allele Identifier: CA1806376425

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101543385T= , CM000670.2:g.101543385T=	GRCh38
NC_000008.10:g.102555613T= , CM000670.1:g.102555613T=	GRCh37
NC_000008.9:g.102624789T=	NCBI36
NG_011971.1:g.55946T=
NG_011971.2:g.55946T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.165T= MANE Select	ENSP00000495564.1:p.Asn55=
ENST00000251808.7:c.165T=	ENSP00000251808.3:p.Asn55=
ENST00000395927.1:c.117T=	ENSP00000379260.1:p.Asn39=
ENST00000472106.2:n.493T=
NM_024915.3:c.165T=	NP_079191.2:p.Asn55=
XM_011517305.1:c.117T=	XP_011515607.1:p.Asn39=
XM_011517306.1:c.117T=	XP_011515608.1:p.Asn39=
XM_011517307.1:c.165T=	XP_011515609.1:p.Asn55=
NM_001330593.1:c.117T=	NP_001317522.1:p.Asn39=
XM_011517306.3:c.117T=	XP_011515608.1:p.Asn39=
XM_011517307.3:c.165T=	XP_011515609.1:p.Asn55=
NM_001330593.2:c.117T=	NP_001317522.1:p.Asn39=
NM_024915.4:c.165T= MANE Select	NP_079191.2:p.Asn55=