Canonical Allele Identifier: CA2648611255

Gene: CFAP45

Linked Data

• gnomAD v4: 1-159886835-ATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159886837_159886838del , CM000663.2:g.159886837_159886838del	GRCh38
NC_000001.10:g.159856627_159856628del , CM000663.1:g.159856627_159856628del	GRCh37
NC_000001.9:g.158123251_158123252del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368099.9:c.589-148_589-147del MANE Select	ENSP00000357079.4:n.589-148_589-147del
ENST00000368099.8:c.589-148_589-147del	ENSP00000357079.4:n.589-148_589-147del
ENST00000426543.6:c.334-148_334-147del	ENSP00000403044.2:n.334-148_334-147del
ENST00000476696.5:c.589-148_589-147del	ENSP00000483972.1:n.589-148_589-147del
ENST00000479940.2:c.334-148_334-147del	ENSP00000478944.1:n.334-148_334-147del
NM_012337.2:c.589-148_589-147del	NP_036469.2:n.589-148_589-147del
NM_012337.3:c.589-148_589-147del MANE Select	NP_036469.2:n.589-148_589-147del