Canonical Allele Identifier: CA1202094317
Gene: CFAP45 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886555T= , CM000663.2:g.159886555T= GRCh38
NC_000001.10:g.159856345T= , CM000663.1:g.159856345T= GRCh37
NC_000001.9:g.158122969T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.723A= MANE Select ENSP00000357079.4:p.Gln241=
ENST00000368099.8:c.723A= ENSP00000357079.4:p.Gln241=
ENST00000426543.6:c.468A= ENSP00000403044.2:p.Gln156=
ENST00000476696.5:c.723A= ENSP00000483972.1:p.Gln241=
NM_012337.2:c.723A= NP_036469.2:p.Gln241=
NM_012337.3:c.723A= MANE Select NP_036469.2:p.Gln241=