Canonical Allele Identifier: CA2635936919

Gene: HES7

Linked Data

• gnomAD v4: 17-8121649-TGGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121656_8121658del , CM000679.2:g.8121656_8121658del	GRCh38
NC_000017.10:g.8024974_8024976del , CM000679.1:g.8024974_8024976del	GRCh37
NC_000017.9:g.7965699_7965701del	NCBI36
NG_015807.1:g.2265_2267del
NG_015816.1:g.7441_7443del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.612_614del MANE Select	ENSP00000446205.2:p.Pro205del
ENST00000317814.8:c.597_599del	ENSP00000314774.4:p.Pro200del
ENST00000541682.6:c.612_614del	ENSP00000446205.2:p.Pro205del
NM_001165967.1:c.612_614del	NP_001159439.1:p.Pro205del
NM_032580.3:c.597_599del	NP_115969.2:p.Pro200del
XM_011524038.1:c.717_719del	XP_011522340.1:p.Pro240del
XM_011524039.1:c.708_710del	XP_011522341.1:p.Pro237del
XM_011524040.1:c.708_710del	XP_011522342.1:p.Pro237del
XM_011524041.1:c.699_701del	XP_011522343.1:p.Pro234del
XM_011524042.1:c.570_572del	XP_011522344.1:p.Pro191del
XR_934203.1:n.69+1842_69+1844del
XM_017025232.1:c.717_719del	XP_016880721.1:p.Pro240del
XM_024451007.1:c.717_719del	XP_024306775.1:p.Pro240del
NM_001165967.2:c.612_614del MANE Select	NP_001159439.1:p.Pro205del
NM_032580.4:c.597_599del	NP_115969.2:p.Pro200del