Canonical Allele Identifier: CA624868619
Gene: HES7 HGNC NCBI

Linked Data

dbSNP Id: rs1399515151

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8121966del , CM000679.2:g.8121966del GRCh38
NC_000017.10:g.8025284del , CM000679.1:g.8025284del GRCh37
NC_000017.9:g.7966009del NCBI36
NG_015807.1:g.1952del
NG_015816.1:g.7128del

Transcript Alleles

HGVS Amino-acid Change
ENST00000541682.7:c.299del MANE Select ENSP00000446205.2:p.Gly100ValfsTer?
ENST00000317814.8:c.284del ENSP00000314774.4:p.Gly95ValfsTer?
ENST00000541682.6:c.299del ENSP00000446205.2:p.Gly100ValfsTer?
ENST00000577735.1:c.275del ENSP00000462491.1:p.Gly92ValfsTer?
NM_001165967.1:c.299del NP_001159439.1:p.Gly100ValfsTer?
NM_032580.3:c.284del NP_115969.2:p.Gly95ValfsTer?
XM_011524038.1:c.404del XP_011522340.1:p.Gly135ValfsTer?
XM_011524039.1:c.395del XP_011522341.1:p.Gly132ValfsTer?
XM_011524040.1:c.395del XP_011522342.1:p.Gly132ValfsTer?
XM_011524041.1:c.386del XP_011522343.1:p.Gly129ValfsTer?
XM_011524042.1:c.257del XP_011522344.1:p.Gly86ValfsTer?
XR_934203.1:n.69+2152del
XM_017025232.1:c.404del XP_016880721.1:p.Gly135ValfsTer?
XM_024451007.1:c.404del XP_024306775.1:p.Gly135ValfsTer?
NM_001165967.2:c.299del MANE Select NP_001159439.1:p.Gly100ValfsTer?
NM_032580.4:c.284del NP_115969.2:p.Gly95ValfsTer?