Canonical Allele Identifier: CA2688131390

Gene: GRHL2

Linked Data

• gnomAD v4: 8-101543198-G-GCT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101543205_101543206dup , CM000670.2:g.101543205_101543206dup	GRCh38
NC_000008.10:g.102555433_102555434dup , CM000670.1:g.102555433_102555434dup	GRCh37
NC_000008.9:g.102624609_102624610dup	NCBI36
NG_011971.1:g.55766_55767dup
NG_011971.2:g.55766_55767dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.21-36_21-35dup MANE Select	ENSP00000495564.1:n.21-36_21-35dup
ENST00000251808.7:c.21-36_21-35dup	ENSP00000251808.3:n.21-36_21-35dup
ENST00000395927.1:c.-28-36_-28-35dup	ENSP00000379260.1:n.-28-36_-28-35dup
ENST00000472106.2:n.349-36_349-35dup
NM_024915.3:c.21-36_21-35dup	NP_079191.2:n.21-36_21-35dup
XM_011517305.1:c.-28-36_-28-35dup	XP_011515607.1:n.-28-36_-28-35dup
XM_011517306.1:c.-28-36_-28-35dup	XP_011515608.1:n.-28-36_-28-35dup
XM_011517307.1:c.21-36_21-35dup	XP_011515609.1:n.21-36_21-35dup
NM_001330593.1:c.-28-36_-28-35dup	NP_001317522.1:n.-28-36_-28-35dup
XM_011517306.3:c.-28-36_-28-35dup	XP_011515608.1:n.-28-36_-28-35dup
XM_011517307.3:c.21-36_21-35dup	XP_011515609.1:n.21-36_21-35dup
NM_001330593.2:c.-28-36_-28-35dup	NP_001317522.1:n.-28-36_-28-35dup
NM_024915.4:c.21-36_21-35dup MANE Select	NP_079191.2:n.21-36_21-35dup