Canonical Allele Identifier: CA1191058
Gene: CFAP45 HGNC NCBI

Linked Data

dbSNP Id: rs761039977

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886539C>G , CM000663.2:g.159886539C>G GRCh38
NC_000001.10:g.159856329C>G , CM000663.1:g.159856329C>G GRCh37
NC_000001.9:g.158122953C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.739G>C MANE Select ENSP00000357079.4:p.Glu247Gln
ENST00000368099.8:c.739G>C ENSP00000357079.4:p.Glu247Gln
ENST00000426543.6:c.484G>C ENSP00000403044.2:p.Glu162Gln
ENST00000476696.5:c.739G>C ENSP00000483972.1:p.Glu247Gln
NM_012337.2:c.739G>C NP_036469.2:p.Glu247Gln
NM_012337.3:c.739G>C MANE Select NP_036469.2:p.Glu247Gln