Canonical Allele Identifier: CA1202094372

Gene: CFAP45

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159886759_159886761delinsCAG , CM000663.2:g.159886759_159886761delinsCAG	GRCh38
NC_000001.10:g.159856549_159856551delinsCAG , CM000663.1:g.159856549_159856551delinsCAG	GRCh37
NC_000001.9:g.158123173_158123175delinsCAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368099.9:c.589-72_589-70delinsCTG MANE Select	ENSP00000357079.4:n.589-72_589-70delinsCTG
ENST00000368099.8:c.589-72_589-70delinsCTG	ENSP00000357079.4:n.589-72_589-70delinsCTG
ENST00000426543.6:c.334-72_334-70delinsCTG	ENSP00000403044.2:n.334-72_334-70delinsCTG
ENST00000476696.5:c.589-72_589-70delinsCTG	ENSP00000483972.1:n.589-72_589-70delinsCTG
ENST00000479940.2:c.334-72_334-70delinsCTG	ENSP00000478944.1:n.334-72_334-70delinsCTG
NM_012337.2:c.589-72_589-70delinsCTG	NP_036469.2:n.589-72_589-70delinsCTG
NM_012337.3:c.589-72_589-70delinsCTG MANE Select	NP_036469.2:n.589-72_589-70delinsCTG