Canonical Allele Identifier: CA1806421570

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101644238C= , CM000670.2:g.101644238C=	GRCh38
NC_000008.10:g.102656466C= , CM000670.1:g.102656466C=	GRCh37
NC_000008.9:g.102725642C=	NCBI36
NG_011971.1:g.156799C=
NG_011971.2:g.156799C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.1612+13C= MANE Select	ENSP00000495564.1:n.1612+13C=
ENST00000251808.7:c.1612+13C=	ENSP00000251808.3:n.1612+13C=
ENST00000395927.1:c.1564+13C=	ENSP00000379260.1:n.1564+13C=
ENST00000474338.1:n.254+13C=
ENST00000517674.5:n.267+13C=
NM_024915.3:c.1612+13C=	NP_079191.2:n.1612+13C=
XM_011517305.1:c.1564+13C=	XP_011515607.1:n.1564+13C=
XM_011517306.1:c.1564+13C=	XP_011515608.1:n.1564+13C=
XM_011517307.1:c.1612+13C=	XP_011515609.1:n.1612+13C=
NM_001330593.1:c.1564+13C=	NP_001317522.1:n.1564+13C=
XM_011517306.3:c.1564+13C=	XP_011515608.1:n.1564+13C=
XM_011517307.3:c.1612+13C=	XP_011515609.1:n.1612+13C=
NM_001330593.2:c.1564+13C=	NP_001317522.1:n.1564+13C=
NM_024915.4:c.1612+13C= MANE Select	NP_079191.2:n.1612+13C=