Canonical Allele Identifier: CA343219828
Gene: CFAP45 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.159856369T>A (hg19) chr1:g.159886579T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886579T>A , CM000663.2:g.159886579T>A GRCh38
NC_000001.10:g.159856369T>A , CM000663.1:g.159856369T>A GRCh37
NC_000001.9:g.158122993T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.699A>T MANE Select ENSP00000357079.4:p.Glu233Asp
ENST00000368099.8:c.699A>T ENSP00000357079.4:p.Glu233Asp
ENST00000426543.6:c.444A>T ENSP00000403044.2:p.Glu148Asp
ENST00000476696.5:c.699A>T ENSP00000483972.1:p.Glu233Asp
NM_012337.2:c.699A>T NP_036469.2:p.Glu233Asp
NM_012337.3:c.699A>T MANE Select NP_036469.2:p.Glu233Asp
Search 100 bp 5'
Search 100 bp 3'