Canonical Allele Identifier: CA1806367939

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101524143T= , CM000670.2:g.101524143T=	GRCh38
NC_000008.10:g.102536371T= , CM000670.1:g.102536371T=	GRCh37
NC_000008.9:g.102605547T=	NCBI36
NG_011971.1:g.36704T=
NG_011971.2:g.36704T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000646743.1:c.21-19098T= MANE Select	ENSP00000495564.1:n.21-19098T=
ENST00000251808.7:c.21-19098T=	ENSP00000251808.3:n.21-19098T=
ENST00000395927.1:c.-28-19098T=	ENSP00000379260.1:n.-28-19098T=
ENST00000472106.2:n.349-19098T=
NM_024915.3:c.21-19098T=	NP_079191.2:n.21-19098T=
XM_011517305.1:c.-28-19098T=	XP_011515607.1:n.-28-19098T=
XM_011517306.1:c.-28-19098T=	XP_011515608.1:n.-28-19098T=
XM_011517307.1:c.21-19098T=	XP_011515609.1:n.21-19098T=
NM_001330593.1:c.-28-19098T=	NP_001317522.1:n.-28-19098T=
XM_011517306.3:c.-28-19098T=	XP_011515608.1:n.-28-19098T=
XM_011517307.3:c.21-19098T=	XP_011515609.1:n.21-19098T=
NM_001330593.2:c.-28-19098T=	NP_001317522.1:n.-28-19098T=
NM_024915.4:c.21-19098T= MANE Select	NP_079191.2:n.21-19098T=