Canonical Allele Identifier: CA343219900
Gene: CFAP45 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.159856400G>T (hg19) chr1:g.159886610G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886610G>T , CM000663.2:g.159886610G>T GRCh38
NC_000001.10:g.159856400G>T , CM000663.1:g.159856400G>T GRCh37
NC_000001.9:g.158123024G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.668C>A MANE Select ENSP00000357079.4:p.Thr223Lys
ENST00000368099.8:c.668C>A ENSP00000357079.4:p.Thr223Lys
ENST00000426543.6:c.413C>A ENSP00000403044.2:p.Thr138Lys
ENST00000476696.5:c.668C>A ENSP00000483972.1:p.Thr223Lys
ENST00000479940.2:c.413C>A ENSP00000478944.1:p.Thr138Lys
NM_012337.2:c.668C>A NP_036469.2:p.Thr223Lys
NM_012337.3:c.668C>A MANE Select NP_036469.2:p.Thr223Lys
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