Canonical Allele Identifier: CA844668522

Gene: GRHL2

Linked Data

• dbSNP Id: rs1270081246
• gnomAD v3: 8-101543228-CTT-C
• gnomAD v4: 8-101543228-CTT-C
• MyVariant Identifiers: chr8:g.102555457_102555458del (hg19) ; chr8:g.101543229_101543230del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101543229_101543230del , CM000670.2:g.101543229_101543230del	GRCh38
NC_000008.10:g.102555457_102555458del , CM000670.1:g.102555457_102555458del	GRCh37
NC_000008.9:g.102624633_102624634del	NCBI36
NG_011971.1:g.55790_55791del
NG_011971.2:g.55790_55791del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.21-12_21-11del MANE Select	ENSP00000495564.1:n.21-12_21-11del
ENST00000251808.7:c.21-12_21-11del	ENSP00000251808.3:n.21-12_21-11del
ENST00000395927.1:c.-28-12_-28-11del	ENSP00000379260.1:n.-28-12_-28-11del
ENST00000472106.2:n.349-12_349-11del
NM_024915.3:c.21-12_21-11del	NP_079191.2:n.21-12_21-11del
XM_011517305.1:c.-28-12_-28-11del	XP_011515607.1:n.-28-12_-28-11del
XM_011517306.1:c.-28-12_-28-11del	XP_011515608.1:n.-28-12_-28-11del
XM_011517307.1:c.21-12_21-11del	XP_011515609.1:n.21-12_21-11del
NM_001330593.1:c.-28-12_-28-11del	NP_001317522.1:n.-28-12_-28-11del
XM_011517306.3:c.-28-12_-28-11del	XP_011515608.1:n.-28-12_-28-11del
XM_011517307.3:c.21-12_21-11del	XP_011515609.1:n.21-12_21-11del
NM_001330593.2:c.-28-12_-28-11del	NP_001317522.1:n.-28-12_-28-11del
NM_024915.4:c.21-12_21-11del MANE Select	NP_079191.2:n.21-12_21-11del