Canonical Allele Identifier: CA1202094306
Gene: CFAP45 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886523T= , CM000663.2:g.159886523T= GRCh38
NC_000001.10:g.159856313T= , CM000663.1:g.159856313T= GRCh37
NC_000001.9:g.158122937T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.755A= MANE Select ENSP00000357079.4:p.Glu252=
ENST00000368099.8:c.755A= ENSP00000357079.4:p.Glu252=
ENST00000426543.6:c.500A= ENSP00000403044.2:p.Glu167=
ENST00000476696.5:c.755A= ENSP00000483972.1:p.Glu252=
NM_012337.2:c.755A= NP_036469.2:p.Glu252=
NM_012337.3:c.755A= MANE Select NP_036469.2:p.Glu252=