Canonical Allele Identifier: CA421350641
Gene: CFAP45 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.159856381A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886591A>G , CM000663.2:g.159886591A>G GRCh38
NC_000001.10:g.159856381A>G , CM000663.1:g.159856381A>G GRCh37
NC_000001.9:g.158123005A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.687T>C MANE Select ENSP00000357079.4:p.Asp229=
ENST00000368099.8:c.687T>C ENSP00000357079.4:p.Asp229=
ENST00000426543.6:c.432T>C ENSP00000403044.2:p.Asp144=
ENST00000476696.5:c.687T>C ENSP00000483972.1:p.Asp229=
NM_012337.2:c.687T>C NP_036469.2:p.Asp229=
NM_012337.3:c.687T>C MANE Select NP_036469.2:p.Asp229=
Search 100 bp 5'
Search 100 bp 3'