Canonical Allele Identifier: CA1147616542

Gene: CFAP45

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159886440T= , CM000663.2:g.159886440T=	GRCh38
NC_000001.10:g.159856230T= , CM000663.1:g.159856230T=	GRCh37
NC_000001.9:g.158122854T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368099.9:c.767+71A= MANE Select	ENSP00000357079.4:n.767+71A=
ENST00000368099.8:c.767+71A=	ENSP00000357079.4:n.767+71A=
ENST00000426543.6:c.512+71A=	ENSP00000403044.2:n.512+71A=
ENST00000476696.5:c.767+71A=	ENSP00000483972.1:n.767+71A=
NM_012337.2:c.767+71A=	NP_036469.2:n.767+71A=
NM_012337.3:c.767+71A= MANE Select	NP_036469.2:n.767+71A=