Canonical Allele Identifier: CA2635936626

Gene: HES7

Linked Data

• gnomAD v4: 17-8121585-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121587del , CM000679.2:g.8121587del	GRCh38
NC_000017.10:g.8024905del , CM000679.1:g.8024905del	GRCh37
NC_000017.9:g.7965630del	NCBI36
NG_015807.1:g.2331del
NG_015816.1:g.7507del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.678del MANE Select	ENSP00000446205.2:p.Trp226Ter
ENST00000317814.8:c.663del	ENSP00000314774.4:p.Trp221Ter
ENST00000541682.6:c.678del	ENSP00000446205.2:p.Trp226Ter
NM_001165967.1:c.678del	NP_001159439.1:p.Trp226Ter
NM_032580.3:c.663del	NP_115969.2:p.Trp221Ter
XM_011524038.1:c.783del	XP_011522340.1:p.Trp261Ter
XM_011524039.1:c.774del	XP_011522341.1:p.Trp258Ter
XM_011524040.1:c.774del	XP_011522342.1:p.Trp258Ter
XM_011524041.1:c.765del	XP_011522343.1:p.Trp255Ter
XM_011524042.1:c.636del	XP_011522344.1:p.Trp212Ter
XR_934203.1:n.69+1773del
XM_017025232.1:c.783del	XP_016880721.1:p.Trp261Ter
XM_024451007.1:c.783del	XP_024306775.1:p.Trp261Ter
NM_001165967.2:c.678del MANE Select	NP_001159439.1:p.Trp226Ter
NM_032580.4:c.663del	NP_115969.2:p.Trp221Ter