Canonical Allele Identifier: CA1806376509

Gene: GRHL2

Linked Data

• dbSNP Id: rs1811199278

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101543557_101543558dup , CM000670.2:g.101543557_101543558dup	GRCh38
NC_000008.10:g.102555785_102555786dup , CM000670.1:g.102555785_102555786dup	GRCh37
NC_000008.9:g.102624961_102624962dup	NCBI36
NG_011971.1:g.56118_56119dup
NG_011971.2:g.56118_56119dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.216+121_216+122dup MANE Select	ENSP00000495564.1:n.216+121_216+122dup
ENST00000251808.7:c.216+121_216+122dup	ENSP00000251808.3:n.216+121_216+122dup
ENST00000395927.1:c.168+121_168+122dup	ENSP00000379260.1:n.168+121_168+122dup
ENST00000472106.2:n.665_666dup
NM_024915.3:c.216+121_216+122dup	NP_079191.2:n.216+121_216+122dup
XM_011517305.1:c.168+121_168+122dup	XP_011515607.1:n.168+121_168+122dup
XM_011517306.1:c.168+121_168+122dup	XP_011515608.1:n.168+121_168+122dup
XM_011517307.1:c.216+121_216+122dup	XP_011515609.1:n.216+121_216+122dup
NM_001330593.1:c.168+121_168+122dup	NP_001317522.1:n.168+121_168+122dup
XM_011517306.3:c.168+121_168+122dup	XP_011515608.1:n.168+121_168+122dup
XM_011517307.3:c.216+121_216+122dup	XP_011515609.1:n.216+121_216+122dup
NM_001330593.2:c.168+121_168+122dup	NP_001317522.1:n.168+121_168+122dup
NM_024915.4:c.216+121_216+122dup MANE Select	NP_079191.2:n.216+121_216+122dup