Canonical Allele Identifier: CA1202094350
Gene: CFAP45 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886693G= , CM000663.2:g.159886693G= GRCh38
NC_000001.10:g.159856483G= , CM000663.1:g.159856483G= GRCh37
NC_000001.9:g.158123107G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.589-4C= MANE Select ENSP00000357079.4:n.589-4C=
ENST00000368099.8:c.589-4C= ENSP00000357079.4:n.589-4C=
ENST00000426543.6:c.334-4C= ENSP00000403044.2:n.334-4C=
ENST00000476696.5:c.589-4C= ENSP00000483972.1:n.589-4C=
ENST00000479940.2:c.334-4C= ENSP00000478944.1:n.334-4C=
NM_012337.2:c.589-4C= NP_036469.2:n.589-4C=
NM_012337.3:c.589-4C= MANE Select NP_036469.2:n.589-4C=
Search 100 bp 5'
Search 100 bp 3'