Canonical Allele Identifier: CA1008314497
Gene: CFAP45 HGNC NCBI

Linked Data

dbSNP Id: rs1649697954

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886761_159886762del , CM000663.2:g.159886761_159886762del GRCh38
NC_000001.10:g.159856551_159856552del , CM000663.1:g.159856551_159856552del GRCh37
NC_000001.9:g.158123175_158123176del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.589-72_589-71del MANE Select ENSP00000357079.4:n.589-72_589-71del
ENST00000368099.8:c.589-72_589-71del ENSP00000357079.4:n.589-72_589-71del
ENST00000426543.6:c.334-72_334-71del ENSP00000403044.2:n.334-72_334-71del
ENST00000476696.5:c.589-72_589-71del ENSP00000483972.1:n.589-72_589-71del
ENST00000479940.2:c.334-72_334-71del ENSP00000478944.1:n.334-72_334-71del
NM_012337.2:c.589-72_589-71del NP_036469.2:n.589-72_589-71del
NM_012337.3:c.589-72_589-71del MANE Select NP_036469.2:n.589-72_589-71del