Canonical Allele Identifier: CA1202094316

Gene: CFAP45

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159886552C= , CM000663.2:g.159886552C=	GRCh38
NC_000001.10:g.159856342C= , CM000663.1:g.159856342C=	GRCh37
NC_000001.9:g.158122966C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368099.9:c.726G= MANE Select	ENSP00000357079.4:p.Arg242=
ENST00000368099.8:c.726G=	ENSP00000357079.4:p.Arg242=
ENST00000426543.6:c.471G=	ENSP00000403044.2:p.Arg157=
ENST00000476696.5:c.726G=	ENSP00000483972.1:p.Arg242=
NM_012337.2:c.726G=	NP_036469.2:p.Arg242=
NM_012337.3:c.726G= MANE Select	NP_036469.2:p.Arg242=