Canonical Allele Identifier: CA2688134417

Gene: GRHL2

Linked Data

• gnomAD v4: 8-101644357-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101644359del , CM000670.2:g.101644359del	GRCh38
NC_000008.10:g.102656587del , CM000670.1:g.102656587del	GRCh37
NC_000008.9:g.102725763del	NCBI36
NG_011971.1:g.156920del
NG_011971.2:g.156920del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.1612+134del MANE Select	ENSP00000495564.1:n.1612+134del
ENST00000251808.7:c.1612+134del	ENSP00000251808.3:n.1612+134del
ENST00000395927.1:c.1564+134del	ENSP00000379260.1:n.1564+134del
ENST00000474338.1:n.254+134del
ENST00000517674.5:n.267+134del
NM_024915.3:c.1612+134del	NP_079191.2:n.1612+134del
XM_011517305.1:c.1564+134del	XP_011515607.1:n.1564+134del
XM_011517306.1:c.1564+134del	XP_011515608.1:n.1564+134del
XM_011517307.1:c.1612+134del	XP_011515609.1:n.1612+134del
NM_001330593.1:c.1564+134del	NP_001317522.1:n.1564+134del
XM_011517306.3:c.1564+134del	XP_011515608.1:n.1564+134del
XM_011517307.3:c.1612+134del	XP_011515609.1:n.1612+134del
NM_001330593.2:c.1564+134del	NP_001317522.1:n.1564+134del
NM_024915.4:c.1612+134del MANE Select	NP_079191.2:n.1612+134del