Canonical Allele Identifier: CA2648610954
Gene: CFAP45 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886399_159886402del , CM000663.2:g.159886399_159886402del GRCh38
NC_000001.10:g.159856189_159856192del , CM000663.1:g.159856189_159856192del GRCh37
NC_000001.9:g.158122813_158122816del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.767+111_767+114del MANE Select ENSP00000357079.4:n.767+111_767+114del
ENST00000368099.8:c.767+111_767+114del ENSP00000357079.4:n.767+111_767+114del
ENST00000426543.6:c.512+111_512+114del ENSP00000403044.2:n.512+111_512+114del
ENST00000476696.5:c.767+111_767+114del ENSP00000483972.1:n.767+111_767+114del
NM_012337.2:c.767+111_767+114del NP_036469.2:n.767+111_767+114del
NM_012337.3:c.767+111_767+114del MANE Select NP_036469.2:n.767+111_767+114del