Canonical Allele Identifier: CA371644197

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101558679A>G , CM000670.2:g.101558679A>G	GRCh38
NC_000008.10:g.102570907A>G , CM000670.1:g.102570907A>G	GRCh37
NC_000008.9:g.102640083A>G	NCBI36
NG_011971.1:g.71240A>G
NG_011971.2:g.71240A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024915.4:c.545A>G MANE Select	NP_079191.2:p.Gln182Arg
ENST00000646743.1:c.545A>G MANE Select	ENSP00000495564.1:p.Gln182Arg
NM_001330593.1:c.497A>G	NP_001317522.1:p.Gln166Arg
NM_001330593.2:c.497A>G	NP_001317522.1:p.Gln166Arg
NM_024915.3:c.545A>G	NP_079191.2:p.Gln182Arg
ENST00000251808.7:c.545A>G	ENSP00000251808.3:p.Gln182Arg
ENST00000395927.1:c.497A>G	ENSP00000379260.1:p.Gln166Arg
XM_011517305.1:c.497A>G	XP_011515607.1:p.Gln166Arg
XM_011517306.1:c.497A>G	XP_011515608.1:p.Gln166Arg
XM_011517306.3:c.497A>G	XP_011515608.1:p.Gln166Arg
XM_011517307.1:c.545A>G	XP_011515609.1:p.Gln182Arg
XM_011517307.3:c.545A>G	XP_011515609.1:p.Gln182Arg