Canonical Allele Identifier: CA2648610957
Gene: CFAP45 HGNC NCBI

Linked Data

gnomAD v4: 1-159886398-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886398A>T , CM000663.2:g.159886398A>T GRCh38
NC_000001.10:g.159856188A>T , CM000663.1:g.159856188A>T GRCh37
NC_000001.9:g.158122812A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.767+113T>A MANE Select ENSP00000357079.4:n.767+113T>A
ENST00000368099.8:c.767+113T>A ENSP00000357079.4:n.767+113T>A
ENST00000426543.6:c.512+113T>A ENSP00000403044.2:n.512+113T>A
ENST00000476696.5:c.767+113T>A ENSP00000483972.1:n.767+113T>A
NM_012337.2:c.767+113T>A NP_036469.2:n.767+113T>A
NM_012337.3:c.767+113T>A MANE Select NP_036469.2:n.767+113T>A
Search 100 bp 5'
Search 100 bp 3'