Canonical Allele Identifier: CA343219918

Gene: CFAP45

Linked Data

• MyVariant Identifiers: chr1:g.159856409T>A (hg19) ; chr1:g.159886619T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159886619T>A , CM000663.2:g.159886619T>A	GRCh38
NC_000001.10:g.159856409T>A , CM000663.1:g.159856409T>A	GRCh37
NC_000001.9:g.158123033T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368099.9:c.659A>T MANE Select	ENSP00000357079.4:p.Glu220Val
ENST00000368099.8:c.659A>T	ENSP00000357079.4:p.Glu220Val
ENST00000426543.6:c.404A>T	ENSP00000403044.2:p.Glu135Val
ENST00000476696.5:c.659A>T	ENSP00000483972.1:p.Glu220Val
ENST00000479940.2:c.404A>T	ENSP00000478944.1:p.Glu135Val
NM_012337.2:c.659A>T	NP_036469.2:p.Glu220Val
NM_012337.3:c.659A>T MANE Select	NP_036469.2:p.Glu220Val