Canonical Allele Identifier: CA1806376373

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101543228_101543230delinsCTT , CM000670.2:g.101543228_101543230delinsCTT	GRCh38
NC_000008.10:g.102555456_102555458delinsCTT , CM000670.1:g.102555456_102555458delinsCTT	GRCh37
NC_000008.9:g.102624632_102624634delinsCTT	NCBI36
NG_011971.1:g.55789_55791delinsCTT
NG_011971.2:g.55789_55791delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.21-13_21-11delinsCTT MANE Select	ENSP00000495564.1:n.21-13_21-11delinsCTT
ENST00000251808.7:c.21-13_21-11delinsCTT	ENSP00000251808.3:n.21-13_21-11delinsCTT
ENST00000395927.1:c.-28-13_-28-11delinsCTT	ENSP00000379260.1:n.-28-13_-28-11delinsCTT
ENST00000472106.2:n.349-13_349-11delinsCTT
NM_024915.3:c.21-13_21-11delinsCTT	NP_079191.2:n.21-13_21-11delinsCTT
XM_011517305.1:c.-28-13_-28-11delinsCTT	XP_011515607.1:n.-28-13_-28-11delinsCTT
XM_011517306.1:c.-28-13_-28-11delinsCTT	XP_011515608.1:n.-28-13_-28-11delinsCTT
XM_011517307.1:c.21-13_21-11delinsCTT	XP_011515609.1:n.21-13_21-11delinsCTT
NM_001330593.1:c.-28-13_-28-11delinsCTT	NP_001317522.1:n.-28-13_-28-11delinsCTT
XM_011517306.3:c.-28-13_-28-11delinsCTT	XP_011515608.1:n.-28-13_-28-11delinsCTT
XM_011517307.3:c.21-13_21-11delinsCTT	XP_011515609.1:n.21-13_21-11delinsCTT
NM_001330593.2:c.-28-13_-28-11delinsCTT	NP_001317522.1:n.-28-13_-28-11delinsCTT
NM_024915.4:c.21-13_21-11delinsCTT MANE Select	NP_079191.2:n.21-13_21-11delinsCTT