Canonical Allele Identifier: CA1202094254

Gene: CFAP45

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159886402_159886403delinsAG , CM000663.2:g.159886402_159886403delinsAG	GRCh38
NC_000001.10:g.159856192_159856193delinsAG , CM000663.1:g.159856192_159856193delinsAG	GRCh37
NC_000001.9:g.158122816_158122817delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368099.9:c.767+108_767+109delinsCT MANE Select	ENSP00000357079.4:n.767+108_767+109delinsCT
ENST00000368099.8:c.767+108_767+109delinsCT	ENSP00000357079.4:n.767+108_767+109delinsCT
ENST00000426543.6:c.512+108_512+109delinsCT	ENSP00000403044.2:n.512+108_512+109delinsCT
ENST00000476696.5:c.767+108_767+109delinsCT	ENSP00000483972.1:n.767+108_767+109delinsCT
NM_012337.2:c.767+108_767+109delinsCT	NP_036469.2:n.767+108_767+109delinsCT
NM_012337.3:c.767+108_767+109delinsCT MANE Select	NP_036469.2:n.767+108_767+109delinsCT