Canonical Allele Identifier: CA2635938703
Gene: HES7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8122031_8122079del , CM000679.2:g.8122031_8122079del GRCh38
NC_000017.10:g.8025349_8025397del , CM000679.1:g.8025349_8025397del GRCh37
NC_000017.9:g.7966074_7966122del NCBI36
NG_015807.1:g.1841_1889del
NG_015816.1:g.7017_7065del

Transcript Alleles

HGVS Amino-acid Change
ENST00000541682.7:c.227-39_236del
ENST00000317814.8:c.227-54_227-6del ENSP00000314774.4:n.227-54_227-6del
ENST00000541682.6:c.227-39_236del
ENST00000577735.1:c.203-39_212del
NM_001165967.1:c.227-39_236del
NM_032580.3:c.227-54_227-6del NP_115969.2:n.227-54_227-6del
XM_011524038.1:c.332-39_341del
XM_011524039.1:c.323-39_332del
XM_011524040.1:c.323-39_332del
XM_011524041.1:c.314-39_323del
XM_011524042.1:c.185-39_194del
XR_934203.1:n.69+2217_69+2265del
XM_017025232.1:c.332-39_341del
XM_024451007.1:c.332-39_341del
NM_001165967.2:c.227-39_236del
NM_032580.4:c.227-54_227-6del NP_115969.2:n.227-54_227-6del