Canonical Allele Identifier: CA2635938977
Gene: HES7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8122104_8122108dup , CM000679.2:g.8122104_8122108dup GRCh38
NC_000017.10:g.8025422_8025426dup , CM000679.1:g.8025422_8025426dup GRCh37
NC_000017.9:g.7966147_7966151dup NCBI36
NG_015807.1:g.1809_1813dup
NG_015816.1:g.6985_6989dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000541682.7:c.227-71_227-67dup MANE Select ENSP00000446205.2:n.227-71_227-67dup
ENST00000317814.8:c.227-86_227-82dup ENSP00000314774.4:n.227-86_227-82dup
ENST00000541682.6:c.227-71_227-67dup ENSP00000446205.2:n.227-71_227-67dup
ENST00000577735.1:c.203-71_203-67dup ENSP00000462491.1:n.203-71_203-67dup
NM_001165967.1:c.227-71_227-67dup NP_001159439.1:n.227-71_227-67dup
NM_032580.3:c.227-86_227-82dup NP_115969.2:n.227-86_227-82dup
XM_011524038.1:c.332-71_332-67dup XP_011522340.1:n.332-71_332-67dup
XM_011524039.1:c.323-71_323-67dup XP_011522341.1:n.323-71_323-67dup
XM_011524040.1:c.323-71_323-67dup XP_011522342.1:n.323-71_323-67dup
XM_011524041.1:c.314-71_314-67dup XP_011522343.1:n.314-71_314-67dup
XM_011524042.1:c.185-71_185-67dup XP_011522344.1:n.185-71_185-67dup
XR_934203.1:n.69+2290_69+2294dup
XM_017025232.1:c.332-71_332-67dup XP_016880721.1:n.332-71_332-67dup
XM_024451007.1:c.332-71_332-67dup XP_024306775.1:n.332-71_332-67dup
NM_001165967.2:c.227-71_227-67dup MANE Select NP_001159439.1:n.227-71_227-67dup
NM_032580.4:c.227-86_227-82dup NP_115969.2:n.227-86_227-82dup