Canonical Allele Identifier: CA2246161085

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8122084_8122085delinsAG , CM000679.2:g.8122084_8122085delinsAG	GRCh38
NC_000017.10:g.8025402_8025403delinsAG , CM000679.1:g.8025402_8025403delinsAG	GRCh37
NC_000017.9:g.7966127_7966128delinsAG	NCBI36
NG_015807.1:g.1832_1833delinsCT
NG_015816.1:g.7008_7009delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.227-48_227-47delinsCT MANE Select	ENSP00000446205.2:n.227-48_227-47delinsCT
ENST00000317814.8:c.227-63_227-62delinsCT	ENSP00000314774.4:n.227-63_227-62delinsCT
ENST00000541682.6:c.227-48_227-47delinsCT	ENSP00000446205.2:n.227-48_227-47delinsCT
ENST00000577735.1:c.203-48_203-47delinsCT	ENSP00000462491.1:n.203-48_203-47delinsCT
NM_001165967.1:c.227-48_227-47delinsCT	NP_001159439.1:n.227-48_227-47delinsCT
NM_032580.3:c.227-63_227-62delinsCT	NP_115969.2:n.227-63_227-62delinsCT
XM_011524038.1:c.332-48_332-47delinsCT	XP_011522340.1:n.332-48_332-47delinsCT
XM_011524039.1:c.323-48_323-47delinsCT	XP_011522341.1:n.323-48_323-47delinsCT
XM_011524040.1:c.323-48_323-47delinsCT	XP_011522342.1:n.323-48_323-47delinsCT
XM_011524041.1:c.314-48_314-47delinsCT	XP_011522343.1:n.314-48_314-47delinsCT
XM_011524042.1:c.185-48_185-47delinsCT	XP_011522344.1:n.185-48_185-47delinsCT
XR_934203.1:n.69+2270_69+2271delinsAG
XM_017025232.1:c.332-48_332-47delinsCT	XP_016880721.1:n.332-48_332-47delinsCT
XM_024451007.1:c.332-48_332-47delinsCT	XP_024306775.1:n.332-48_332-47delinsCT
NM_001165967.2:c.227-48_227-47delinsCT MANE Select	NP_001159439.1:n.227-48_227-47delinsCT
NM_032580.4:c.227-63_227-62delinsCT	NP_115969.2:n.227-63_227-62delinsCT