Canonical Allele Identifier: CA1146917021
Gene: CFAP45 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886823G= , CM000663.2:g.159886823G= GRCh38
NC_000001.10:g.159856613G= , CM000663.1:g.159856613G= GRCh37
NC_000001.9:g.158123237G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.589-134C= MANE Select ENSP00000357079.4:n.589-134C=
ENST00000368099.8:c.589-134C= ENSP00000357079.4:n.589-134C=
ENST00000426543.6:c.334-134C= ENSP00000403044.2:n.334-134C=
ENST00000476696.5:c.589-134C= ENSP00000483972.1:n.589-134C=
ENST00000479940.2:c.334-134C= ENSP00000478944.1:n.334-134C=
NM_012337.2:c.589-134C= NP_036469.2:n.589-134C=
NM_012337.3:c.589-134C= MANE Select NP_036469.2:n.589-134C=
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