Canonical Allele Identifier: CA2580078494

Gene: GRHL2

Linked Data

• ClinVar Variation Id: 2440600
• ClinVar RCV Id: RCV003145901

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101644129del , CM000670.2:g.101644129del	GRCh38
NC_000008.10:g.102656357del , CM000670.1:g.102656357del	GRCh37
NC_000008.9:g.102725533del	NCBI36
NG_011971.1:g.156690del
NG_011971.2:g.156690del

Transcript Alleles

HGVS	Amino-acid change
ENST00000646743.1:c.1518-2del MANE Select	ENSP00000495564.1:n.1518-2del
ENST00000251808.7:c.1518-2del	ENSP00000251808.3:n.1518-2del
ENST00000395927.1:c.1470-2del	ENSP00000379260.1:n.1470-2del
ENST00000474338.1:n.160-2del
ENST00000517674.5:n.173-2del
NM_024915.3:c.1518-2del	NP_079191.2:n.1518-2del
XM_011517305.1:c.1470-2del	XP_011515607.1:n.1470-2del
XM_011517306.1:c.1470-2del	XP_011515608.1:n.1470-2del
XM_011517307.1:c.1518-2del	XP_011515609.1:n.1518-2del
NM_001330593.1:c.1470-2del	NP_001317522.1:n.1470-2del
XM_011517306.3:c.1470-2del	XP_011515608.1:n.1470-2del
XM_011517307.3:c.1518-2del	XP_011515609.1:n.1518-2del
NM_001330593.2:c.1470-2del	NP_001317522.1:n.1470-2del
NM_024915.4:c.1518-2del MANE Select	NP_079191.2:n.1518-2del