Canonical Allele Identifier: CA2635938956

Gene: HES7

Linked Data

• gnomAD v4: 17-8122096-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8122100del , CM000679.2:g.8122100del	GRCh38
NC_000017.10:g.8025418del , CM000679.1:g.8025418del	GRCh37
NC_000017.9:g.7966143del	NCBI36
NG_015807.1:g.1820del
NG_015816.1:g.6996del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.227-60del MANE Select	ENSP00000446205.2:n.227-60del
ENST00000317814.8:c.227-75del	ENSP00000314774.4:n.227-75del
ENST00000541682.6:c.227-60del	ENSP00000446205.2:n.227-60del
ENST00000577735.1:c.203-60del	ENSP00000462491.1:n.203-60del
NM_001165967.1:c.227-60del	NP_001159439.1:n.227-60del
NM_032580.3:c.227-75del	NP_115969.2:n.227-75del
XM_011524038.1:c.332-60del	XP_011522340.1:n.332-60del
XM_011524039.1:c.323-60del	XP_011522341.1:n.323-60del
XM_011524040.1:c.323-60del	XP_011522342.1:n.323-60del
XM_011524041.1:c.314-60del	XP_011522343.1:n.314-60del
XM_011524042.1:c.185-60del	XP_011522344.1:n.185-60del
XR_934203.1:n.69+2286del
XM_017025232.1:c.332-60del	XP_016880721.1:n.332-60del
XM_024451007.1:c.332-60del	XP_024306775.1:n.332-60del
NM_001165967.2:c.227-60del MANE Select	NP_001159439.1:n.227-60del
NM_032580.4:c.227-75del	NP_115969.2:n.227-75del