Canonical Allele Identifier: CA1202094270
Gene: CFAP45 HGNC NCBI

Linked Data

dbSNP Id: rs1649687878

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886428del , CM000663.2:g.159886428del GRCh38
NC_000001.10:g.159856218del , CM000663.1:g.159856218del GRCh37
NC_000001.9:g.158122842del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.767+83del MANE Select ENSP00000357079.4:n.767+83del
ENST00000368099.8:c.767+83del ENSP00000357079.4:n.767+83del
ENST00000426543.6:c.512+83del ENSP00000403044.2:n.512+83del
ENST00000476696.5:c.767+83del ENSP00000483972.1:n.767+83del
NM_012337.2:c.767+83del NP_036469.2:n.767+83del
NM_012337.3:c.767+83del MANE Select NP_036469.2:n.767+83del