Canonical Allele Identifier: CA2635938895

Gene: HES7

Linked Data

• gnomAD v4: 17-8122080-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8122080_8122081insAG , CM000679.2:g.8122080_8122081insAG	GRCh38
NC_000017.10:g.8025398_8025399insAG , CM000679.1:g.8025398_8025399insAG	GRCh37
NC_000017.9:g.7966123_7966124insAG	NCBI36
NG_015807.1:g.1836_1837insCT
NG_015816.1:g.7012_7013insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.227-44_227-43insCT MANE Select	ENSP00000446205.2:n.227-44_227-43insCT
ENST00000317814.8:c.227-59_227-58insCT	ENSP00000314774.4:n.227-59_227-58insCT
ENST00000541682.6:c.227-44_227-43insCT	ENSP00000446205.2:n.227-44_227-43insCT
ENST00000577735.1:c.203-44_203-43insCT	ENSP00000462491.1:n.203-44_203-43insCT
NM_001165967.1:c.227-44_227-43insCT	NP_001159439.1:n.227-44_227-43insCT
NM_032580.3:c.227-59_227-58insCT	NP_115969.2:n.227-59_227-58insCT
XM_011524038.1:c.332-44_332-43insCT	XP_011522340.1:n.332-44_332-43insCT
XM_011524039.1:c.323-44_323-43insCT	XP_011522341.1:n.323-44_323-43insCT
XM_011524040.1:c.323-44_323-43insCT	XP_011522342.1:n.323-44_323-43insCT
XM_011524041.1:c.314-44_314-43insCT	XP_011522343.1:n.314-44_314-43insCT
XM_011524042.1:c.185-44_185-43insCT	XP_011522344.1:n.185-44_185-43insCT
XR_934203.1:n.69+2266_69+2267insAG
XM_017025232.1:c.332-44_332-43insCT	XP_016880721.1:n.332-44_332-43insCT
XM_024451007.1:c.332-44_332-43insCT	XP_024306775.1:n.332-44_332-43insCT
NM_001165967.2:c.227-44_227-43insCT MANE Select	NP_001159439.1:n.227-44_227-43insCT
NM_032580.4:c.227-59_227-58insCT	NP_115969.2:n.227-59_227-58insCT