Canonical Allele Identifier: CA2573933842
Gene: CFAP45 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886432T>A , CM000663.2:g.159886432T>A GRCh38
NC_000001.10:g.159856222T>A , CM000663.1:g.159856222T>A GRCh37
NC_000001.9:g.158122846T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.767+79A>T MANE Select ENSP00000357079.4:n.767+79A>T
ENST00000368099.8:c.767+79A>T ENSP00000357079.4:n.767+79A>T
ENST00000426543.6:c.512+79A>T ENSP00000403044.2:n.512+79A>T
ENST00000476696.5:c.767+79A>T ENSP00000483972.1:n.767+79A>T
NM_012337.2:c.767+79A>T NP_036469.2:n.767+79A>T
NM_012337.3:c.767+79A>T MANE Select NP_036469.2:n.767+79A>T