Canonical Allele Identifier: CA421350653
Gene: CFAP45 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.159856399T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886609T>C , CM000663.2:g.159886609T>C GRCh38
NC_000001.10:g.159856399T>C , CM000663.1:g.159856399T>C GRCh37
NC_000001.9:g.158123023T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.669A>G MANE Select ENSP00000357079.4:p.Thr223=
ENST00000368099.8:c.669A>G ENSP00000357079.4:p.Thr223=
ENST00000426543.6:c.414A>G ENSP00000403044.2:p.Thr138=
ENST00000476696.5:c.669A>G ENSP00000483972.1:p.Thr223=
ENST00000479940.2:c.414A>G ENSP00000478944.1:p.Thr138=
NM_012337.2:c.669A>G NP_036469.2:p.Thr223=
NM_012337.3:c.669A>G MANE Select NP_036469.2:p.Thr223=
Search 100 bp 5'
Search 100 bp 3'