Canonical Allele Identifier: CA1202094277
Gene: CFAP45 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886461A= , CM000663.2:g.159886461A= GRCh38
NC_000001.10:g.159856251A= , CM000663.1:g.159856251A= GRCh37
NC_000001.9:g.158122875A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.767+50T= MANE Select ENSP00000357079.4:n.767+50T=
ENST00000368099.8:c.767+50T= ENSP00000357079.4:n.767+50T=
ENST00000426543.6:c.512+50T= ENSP00000403044.2:n.512+50T=
ENST00000476696.5:c.767+50T= ENSP00000483972.1:n.767+50T=
NM_012337.2:c.767+50T= NP_036469.2:n.767+50T=
NM_012337.3:c.767+50T= MANE Select NP_036469.2:n.767+50T=