Canonical Allele Identifier: CA2688134337

Gene: GRHL2

Linked Data

• gnomAD v4: 8-101644246-TGCCCTCTCAGAAGGGATGCGGGGTGTCTCTCCCAAGAAGAGCTTGCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101644254_101644300del , CM000670.2:g.101644254_101644300del	GRCh38
NC_000008.10:g.102656482_102656528del , CM000670.1:g.102656482_102656528del	GRCh37
NC_000008.9:g.102725658_102725704del	NCBI36
NG_011971.1:g.156815_156861del
NG_011971.2:g.156815_156861del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.1612+29_1612+75del MANE Select	ENSP00000495564.1:n.1612+29_1612+75del
ENST00000251808.7:c.1612+29_1612+75del	ENSP00000251808.3:n.1612+29_1612+75del
ENST00000395927.1:c.1564+29_1564+75del	ENSP00000379260.1:n.1564+29_1564+75del
ENST00000474338.1:n.254+29_254+75del
ENST00000517674.5:n.267+29_267+75del
NM_024915.3:c.1612+29_1612+75del	NP_079191.2:n.1612+29_1612+75del
XM_011517305.1:c.1564+29_1564+75del	XP_011515607.1:n.1564+29_1564+75del
XM_011517306.1:c.1564+29_1564+75del	XP_011515608.1:n.1564+29_1564+75del
XM_011517307.1:c.1612+29_1612+75del	XP_011515609.1:n.1612+29_1612+75del
NM_001330593.1:c.1564+29_1564+75del	NP_001317522.1:n.1564+29_1564+75del
XM_011517306.3:c.1564+29_1564+75del	XP_011515608.1:n.1564+29_1564+75del
XM_011517307.3:c.1612+29_1612+75del	XP_011515609.1:n.1612+29_1612+75del
NM_001330593.2:c.1564+29_1564+75del	NP_001317522.1:n.1564+29_1564+75del
NM_024915.4:c.1612+29_1612+75del MANE Select	NP_079191.2:n.1612+29_1612+75del