Canonical Allele Identifier: CA2648611243

Gene: CFAP45

Linked Data

• gnomAD v4: 1-159886818-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159886818_159886819insT , CM000663.2:g.159886818_159886819insT	GRCh38
NC_000001.10:g.159856608_159856609insT , CM000663.1:g.159856608_159856609insT	GRCh37
NC_000001.9:g.158123232_158123233insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368099.9:c.589-130_589-129insA MANE Select	ENSP00000357079.4:n.589-130_589-129insA
ENST00000368099.8:c.589-130_589-129insA	ENSP00000357079.4:n.589-130_589-129insA
ENST00000426543.6:c.334-130_334-129insA	ENSP00000403044.2:n.334-130_334-129insA
ENST00000476696.5:c.589-130_589-129insA	ENSP00000483972.1:n.589-130_589-129insA
ENST00000479940.2:c.334-130_334-129insA	ENSP00000478944.1:n.334-130_334-129insA
NM_012337.2:c.589-130_589-129insA	NP_036469.2:n.589-130_589-129insA
NM_012337.3:c.589-130_589-129insA MANE Select	NP_036469.2:n.589-130_589-129insA