Canonical Allele Identifier: CA182750570

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101577191dup , CM000670.2:g.101577191dup	GRCh38
NC_000008.10:g.102589419dup , CM000670.1:g.102589419dup	GRCh37
NC_000008.9:g.102658595dup	NCBI36
NG_011971.1:g.89752dup
NG_011971.2:g.89752dup

Transcript Alleles

HGVS	Amino-acid Change
NM_024915.4:c.892-217dup MANE Select	NP_079191.2:n.892-217dup
ENST00000646743.1:c.892-217dup MANE Select	ENSP00000495564.1:n.892-217dup
NM_001330593.1:c.844-217dup	NP_001317522.1:n.844-217dup
NM_001330593.2:c.844-217dup	NP_001317522.1:n.844-217dup
NM_024915.3:c.892-217dup	NP_079191.2:n.892-217dup
ENST00000251808.7:c.892-217dup	ENSP00000251808.3:n.892-217dup
ENST00000395927.1:c.844-217dup	ENSP00000379260.1:n.844-217dup
XM_011517305.1:c.844-217dup	XP_011515607.1:n.844-217dup
XM_011517306.1:c.844-217dup	XP_011515608.1:n.844-217dup
XM_011517306.3:c.844-217dup	XP_011515608.1:n.844-217dup
XM_011517307.1:c.892-217dup	XP_011515609.1:n.892-217dup
XM_011517307.3:c.892-217dup	XP_011515609.1:n.892-217dup