Canonical Allele Identifier: CA2688131437

Gene: GRHL2

Linked Data

• gnomAD v4: 8-101543518-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101543521del , CM000670.2:g.101543521del	GRCh38
NC_000008.10:g.102555749del , CM000670.1:g.102555749del	GRCh37
NC_000008.9:g.102624925del	NCBI36
NG_011971.1:g.56082del
NG_011971.2:g.56082del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.216+85del MANE Select	ENSP00000495564.1:n.216+85del
ENST00000251808.7:c.216+85del	ENSP00000251808.3:n.216+85del
ENST00000395927.1:c.168+85del	ENSP00000379260.1:n.168+85del
ENST00000472106.2:n.629del
NM_024915.3:c.216+85del	NP_079191.2:n.216+85del
XM_011517305.1:c.168+85del	XP_011515607.1:n.168+85del
XM_011517306.1:c.168+85del	XP_011515608.1:n.168+85del
XM_011517307.1:c.216+85del	XP_011515609.1:n.216+85del
NM_001330593.1:c.168+85del	NP_001317522.1:n.168+85del
XM_011517306.3:c.168+85del	XP_011515608.1:n.168+85del
XM_011517307.3:c.216+85del	XP_011515609.1:n.216+85del
NM_001330593.2:c.168+85del	NP_001317522.1:n.168+85del
NM_024915.4:c.216+85del MANE Select	NP_079191.2:n.216+85del