Canonical Allele Identifier: CA2553879404
Gene: HES7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8122077_8122078insGT , CM000679.2:g.8122077_8122078insGT GRCh38
NC_000017.10:g.8025395_8025396insGT , CM000679.1:g.8025395_8025396insGT GRCh37
NC_000017.9:g.7966120_7966121insGT NCBI36
NG_015807.1:g.1839_1840insAC
NG_015816.1:g.7015_7016insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000541682.7:c.227-41_227-40insAC MANE Select ENSP00000446205.2:n.227-41_227-40insAC
ENST00000317814.8:c.227-56_227-55insAC ENSP00000314774.4:n.227-56_227-55insAC
ENST00000541682.6:c.227-41_227-40insAC ENSP00000446205.2:n.227-41_227-40insAC
ENST00000577735.1:c.203-41_203-40insAC ENSP00000462491.1:n.203-41_203-40insAC
NM_001165967.1:c.227-41_227-40insAC NP_001159439.1:n.227-41_227-40insAC
NM_032580.3:c.227-56_227-55insAC NP_115969.2:n.227-56_227-55insAC
XM_011524038.1:c.332-41_332-40insAC XP_011522340.1:n.332-41_332-40insAC
XM_011524039.1:c.323-41_323-40insAC XP_011522341.1:n.323-41_323-40insAC
XM_011524040.1:c.323-41_323-40insAC XP_011522342.1:n.323-41_323-40insAC
XM_011524041.1:c.314-41_314-40insAC XP_011522343.1:n.314-41_314-40insAC
XM_011524042.1:c.185-41_185-40insAC XP_011522344.1:n.185-41_185-40insAC
XR_934203.1:n.69+2263_69+2264insGT
XM_017025232.1:c.332-41_332-40insAC XP_016880721.1:n.332-41_332-40insAC
XM_024451007.1:c.332-41_332-40insAC XP_024306775.1:n.332-41_332-40insAC
NM_001165967.2:c.227-41_227-40insAC MANE Select NP_001159439.1:n.227-41_227-40insAC
NM_032580.4:c.227-56_227-55insAC NP_115969.2:n.227-56_227-55insAC