Canonical Allele Identifier: CA2576161681

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8122071del , CM000679.2:g.8122071del	GRCh38
NC_000017.10:g.8025389del , CM000679.1:g.8025389del	GRCh37
NC_000017.9:g.7966114del	NCBI36
NG_015807.1:g.1848del
NG_015816.1:g.7024del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.227-32del MANE Select	ENSP00000446205.2:n.227-32del
ENST00000317814.8:c.227-47del	ENSP00000314774.4:n.227-47del
ENST00000541682.6:c.227-32del	ENSP00000446205.2:n.227-32del
ENST00000577735.1:c.203-32del	ENSP00000462491.1:n.203-32del
NM_001165967.1:c.227-32del	NP_001159439.1:n.227-32del
NM_032580.3:c.227-47del	NP_115969.2:n.227-47del
XM_011524038.1:c.332-32del	XP_011522340.1:n.332-32del
XM_011524039.1:c.323-32del	XP_011522341.1:n.323-32del
XM_011524040.1:c.323-32del	XP_011522342.1:n.323-32del
XM_011524041.1:c.314-32del	XP_011522343.1:n.314-32del
XM_011524042.1:c.185-32del	XP_011522344.1:n.185-32del
XR_934203.1:n.69+2257del
XM_017025232.1:c.332-32del	XP_016880721.1:n.332-32del
XM_024451007.1:c.332-32del	XP_024306775.1:n.332-32del
NM_001165967.2:c.227-32del MANE Select	NP_001159439.1:n.227-32del
NM_032580.4:c.227-47del	NP_115969.2:n.227-47del