Canonical Allele Identifier: CA31389831
Gene: CFAP45 HGNC NCBI

Linked Data

dbSNP Id: rs929991076
MyVariant Identifiers: chr1:g.159856549C>G (hg19) chr1:g.159886759C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886759C>G , CM000663.2:g.159886759C>G GRCh38
NC_000001.10:g.159856549C>G , CM000663.1:g.159856549C>G GRCh37
NC_000001.9:g.158123173C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.589-70G>C MANE Select ENSP00000357079.4:n.589-70G>C
ENST00000368099.8:c.589-70G>C ENSP00000357079.4:n.589-70G>C
ENST00000426543.6:c.334-70G>C ENSP00000403044.2:n.334-70G>C
ENST00000476696.5:c.589-70G>C ENSP00000483972.1:n.589-70G>C
ENST00000479940.2:c.334-70G>C ENSP00000478944.1:n.334-70G>C
NM_012337.2:c.589-70G>C NP_036469.2:n.589-70G>C
NM_012337.3:c.589-70G>C MANE Select NP_036469.2:n.589-70G>C
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