Canonical Allele Identifier: CA343219917
Gene: CFAP45 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886618T>G , CM000663.2:g.159886618T>G GRCh38
NC_000001.10:g.159856408T>G , CM000663.1:g.159856408T>G GRCh37
NC_000001.9:g.158123032T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.660A>C MANE Select ENSP00000357079.4:p.Glu220Asp
ENST00000368099.8:c.660A>C ENSP00000357079.4:p.Glu220Asp
ENST00000426543.6:c.405A>C ENSP00000403044.2:p.Glu135Asp
ENST00000476696.5:c.660A>C ENSP00000483972.1:p.Glu220Asp
ENST00000479940.2:c.405A>C ENSP00000478944.1:p.Glu135Asp
NM_012337.2:c.660A>C NP_036469.2:p.Glu220Asp
NM_012337.3:c.660A>C MANE Select NP_036469.2:p.Glu220Asp