Canonical Allele Identifier: CA1142293941

Gene: CFAP45

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159886684G= , CM000663.2:g.159886684G=	GRCh38
NC_000001.10:g.159856474G= , CM000663.1:g.159856474G=	GRCh37
NC_000001.9:g.158123098G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368099.9:c.594C= MANE Select	ENSP00000357079.4:p.Ile198=
ENST00000368099.8:c.594C=	ENSP00000357079.4:p.Ile198=
ENST00000426543.6:c.339C=	ENSP00000403044.2:p.Ile113=
ENST00000476696.5:c.594C=	ENSP00000483972.1:p.Ile198=
ENST00000479940.2:c.339C=	ENSP00000478944.1:p.Ile113=
NM_012337.2:c.594C=	NP_036469.2:p.Ile198=
NM_012337.3:c.594C= MANE Select	NP_036469.2:p.Ile198=