Canonical Allele Identifier: CA1202094329

Gene: CFAP45

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159886611T= , CM000663.2:g.159886611T=	GRCh38
NC_000001.10:g.159856401T= , CM000663.1:g.159856401T=	GRCh37
NC_000001.9:g.158123025T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368099.9:c.667A= MANE Select	ENSP00000357079.4:p.Thr223=
ENST00000368099.8:c.667A=	ENSP00000357079.4:p.Thr223=
ENST00000426543.6:c.412A=	ENSP00000403044.2:p.Thr138=
ENST00000476696.5:c.667A=	ENSP00000483972.1:p.Thr223=
ENST00000479940.2:c.412A=	ENSP00000478944.1:p.Thr138=
NM_012337.2:c.667A=	NP_036469.2:p.Thr223=
NM_012337.3:c.667A= MANE Select	NP_036469.2:p.Thr223=