Canonical Allele Identifier: CA2635936647

Gene: HES7

Linked Data

• gnomAD v4: 17-8121594-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121597del , CM000679.2:g.8121597del	GRCh38
NC_000017.10:g.8024915del , CM000679.1:g.8024915del	GRCh37
NC_000017.9:g.7965640del	NCBI36
NG_015807.1:g.2322del
NG_015816.1:g.7498del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.669del MANE Select	ENSP00000446205.2:p.Ala224LeufsTer?
ENST00000317814.8:c.654del	ENSP00000314774.4:p.Ala219LeufsTer?
ENST00000541682.6:c.669del	ENSP00000446205.2:p.Ala224LeufsTer?
NM_001165967.1:c.669del	NP_001159439.1:p.Ala224LeufsTer?
NM_032580.3:c.654del	NP_115969.2:p.Ala219LeufsTer?
XM_011524038.1:c.774del	XP_011522340.1:p.Ala259LeufsTer?
XM_011524039.1:c.765del	XP_011522341.1:p.Ala256LeufsTer?
XM_011524040.1:c.765del	XP_011522342.1:p.Ala256LeufsTer?
XM_011524041.1:c.756del	XP_011522343.1:p.Ala253LeufsTer?
XM_011524042.1:c.627del	XP_011522344.1:p.Ala210LeufsTer?
XR_934203.1:n.69+1783del
XM_017025232.1:c.774del	XP_016880721.1:p.Ala259LeufsTer?
XM_024451007.1:c.774del	XP_024306775.1:p.Ala259LeufsTer?
NM_001165967.2:c.669del MANE Select	NP_001159439.1:p.Ala224LeufsTer?
NM_032580.4:c.654del	NP_115969.2:p.Ala219LeufsTer?