Canonical Allele Identifier: CA343219625
Gene: CFAP45 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.159856300C>G (hg19) chr1:g.159886510C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886510C>G , CM000663.2:g.159886510C>G GRCh38
NC_000001.10:g.159856300C>G , CM000663.1:g.159856300C>G GRCh37
NC_000001.9:g.158122924C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.767+1G>C MANE Select ENSP00000357079.4:n.767+1G>C
ENST00000368099.8:c.767+1G>C ENSP00000357079.4:n.767+1G>C
ENST00000426543.6:c.512+1G>C ENSP00000403044.2:n.512+1G>C
ENST00000476696.5:c.767+1G>C ENSP00000483972.1:n.767+1G>C
NM_012337.2:c.767+1G>C NP_036469.2:n.767+1G>C
NM_012337.3:c.767+1G>C MANE Select NP_036469.2:n.767+1G>C
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