Canonical Allele Identifier: CA2648610902
Gene: CFAP45 HGNC NCBI

Linked Data

gnomAD v4: 1-159886361-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886361T>G , CM000663.2:g.159886361T>G GRCh38
NC_000001.10:g.159856151T>G , CM000663.1:g.159856151T>G GRCh37
NC_000001.9:g.158122775T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.767+150A>C MANE Select ENSP00000357079.4:n.767+150A>C
ENST00000368099.8:c.767+150A>C ENSP00000357079.4:n.767+150A>C
ENST00000426543.6:c.512+150A>C ENSP00000403044.2:n.512+150A>C
ENST00000476696.5:c.767+150A>C ENSP00000483972.1:n.767+150A>C
NM_012337.2:c.767+150A>C NP_036469.2:n.767+150A>C
NM_012337.3:c.767+150A>C MANE Select NP_036469.2:n.767+150A>C
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