Canonical Allele Identifier: CA1148476085
Gene: CFAP45 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886517C= , CM000663.2:g.159886517C= GRCh38
NC_000001.10:g.159856307C= , CM000663.1:g.159856307C= GRCh37
NC_000001.9:g.158122931C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.761G= MANE Select ENSP00000357079.4:p.Arg254=
ENST00000368099.8:c.761G= ENSP00000357079.4:p.Arg254=
ENST00000426543.6:c.506G= ENSP00000403044.2:p.Arg169=
ENST00000476696.5:c.761G= ENSP00000483972.1:p.Arg254=
NM_012337.2:c.761G= NP_036469.2:p.Arg254=
NM_012337.3:c.761G= MANE Select NP_036469.2:p.Arg254=