Canonical Allele Identifier: CA1806376512

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101543568C= , CM000670.2:g.101543568C=	GRCh38
NC_000008.10:g.102555796C= , CM000670.1:g.102555796C=	GRCh37
NC_000008.9:g.102624972C=	NCBI36
NG_011971.1:g.56129C=
NG_011971.2:g.56129C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.216+132C= MANE Select	ENSP00000495564.1:n.216+132C=
ENST00000251808.7:c.216+132C=	ENSP00000251808.3:n.216+132C=
ENST00000395927.1:c.168+132C=	ENSP00000379260.1:n.168+132C=
ENST00000472106.2:n.676C=
NM_024915.3:c.216+132C=	NP_079191.2:n.216+132C=
XM_011517305.1:c.168+132C=	XP_011515607.1:n.168+132C=
XM_011517306.1:c.168+132C=	XP_011515608.1:n.168+132C=
XM_011517307.1:c.216+132C=	XP_011515609.1:n.216+132C=
NM_001330593.1:c.168+132C=	NP_001317522.1:n.168+132C=
XM_011517306.3:c.168+132C=	XP_011515608.1:n.168+132C=
XM_011517307.3:c.216+132C=	XP_011515609.1:n.216+132C=
NM_001330593.2:c.168+132C=	NP_001317522.1:n.168+132C=
NM_024915.4:c.216+132C= MANE Select	NP_079191.2:n.216+132C=