Canonical Allele Identifier: CA2648611199
Gene: CFAP45 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886768_159886770del , CM000663.2:g.159886768_159886770del GRCh38
NC_000001.10:g.159856558_159856560del , CM000663.1:g.159856558_159856560del GRCh37
NC_000001.9:g.158123182_158123184del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.589-81_589-79del MANE Select ENSP00000357079.4:n.589-81_589-79del
ENST00000368099.8:c.589-81_589-79del ENSP00000357079.4:n.589-81_589-79del
ENST00000426543.6:c.334-81_334-79del ENSP00000403044.2:n.334-81_334-79del
ENST00000476696.5:c.589-81_589-79del ENSP00000483972.1:n.589-81_589-79del
ENST00000479940.2:c.334-81_334-79del ENSP00000478944.1:n.334-81_334-79del
NM_012337.2:c.589-81_589-79del NP_036469.2:n.589-81_589-79del
NM_012337.3:c.589-81_589-79del MANE Select NP_036469.2:n.589-81_589-79del