Canonical Allele Identifier: CA1202094322
Gene: CFAP45 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886577A= , CM000663.2:g.159886577A= GRCh38
NC_000001.10:g.159856367A= , CM000663.1:g.159856367A= GRCh37
NC_000001.9:g.158122991A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.701T= MANE Select ENSP00000357079.4:p.Val234=
ENST00000368099.8:c.701T= ENSP00000357079.4:p.Val234=
ENST00000426543.6:c.446T= ENSP00000403044.2:p.Val149=
ENST00000476696.5:c.701T= ENSP00000483972.1:p.Val234=
NM_012337.2:c.701T= NP_036469.2:p.Val234=
NM_012337.3:c.701T= MANE Select NP_036469.2:p.Val234=