Canonical Allele Identifier: CA2648610962
Gene: CFAP45 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886409_159886417del , CM000663.2:g.159886409_159886417del GRCh38
NC_000001.10:g.159856199_159856207del , CM000663.1:g.159856199_159856207del GRCh37
NC_000001.9:g.158122823_158122831del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.767+99_767+107del MANE Select ENSP00000357079.4:n.767+99_767+107del
ENST00000368099.8:c.767+99_767+107del ENSP00000357079.4:n.767+99_767+107del
ENST00000426543.6:c.512+99_512+107del ENSP00000403044.2:n.512+99_512+107del
ENST00000476696.5:c.767+99_767+107del ENSP00000483972.1:n.767+99_767+107del
NM_012337.2:c.767+99_767+107del NP_036469.2:n.767+99_767+107del
NM_012337.3:c.767+99_767+107del MANE Select NP_036469.2:n.767+99_767+107del