Canonical Allele Identifier: CA182748604

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101558251T>G , CM000670.2:g.101558251T>G	GRCh38
NC_000008.10:g.102570479T>G , CM000670.1:g.102570479T>G	GRCh37
NC_000008.9:g.102639655T>G	NCBI36
NG_011971.1:g.70812T>G
NG_011971.2:g.70812T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024915.4:c.285-168T>G MANE Select	NP_079191.2:n.285-168T>G
ENST00000646743.1:c.285-168T>G MANE Select	ENSP00000495564.1:n.285-168T>G
NM_001330593.1:c.237-168T>G	NP_001317522.1:n.237-168T>G
NM_001330593.2:c.237-168T>G	NP_001317522.1:n.237-168T>G
NM_024915.3:c.285-168T>G	NP_079191.2:n.285-168T>G
ENST00000251808.7:c.285-168T>G	ENSP00000251808.3:n.285-168T>G
ENST00000395927.1:c.237-168T>G	ENSP00000379260.1:n.237-168T>G
XM_011517305.1:c.237-168T>G	XP_011515607.1:n.237-168T>G
XM_011517306.1:c.237-168T>G	XP_011515608.1:n.237-168T>G
XM_011517306.3:c.237-168T>G	XP_011515608.1:n.237-168T>G
XM_011517307.1:c.285-168T>G	XP_011515609.1:n.285-168T>G
XM_011517307.3:c.285-168T>G	XP_011515609.1:n.285-168T>G