Canonical Allele Identifier: CA1202094358
Gene: CFAP45 HGNC NCBI

Linked Data

dbSNP Id: rs1649697006

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886727G>A , CM000663.2:g.159886727G>A GRCh38
NC_000001.10:g.159856517G>A , CM000663.1:g.159856517G>A GRCh37
NC_000001.9:g.158123141G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.589-38C>T MANE Select ENSP00000357079.4:n.589-38C>T
ENST00000368099.8:c.589-38C>T ENSP00000357079.4:n.589-38C>T
ENST00000426543.6:c.334-38C>T ENSP00000403044.2:n.334-38C>T
ENST00000476696.5:c.589-38C>T ENSP00000483972.1:n.589-38C>T
ENST00000479940.2:c.334-38C>T ENSP00000478944.1:n.334-38C>T
NM_012337.2:c.589-38C>T NP_036469.2:n.589-38C>T
NM_012337.3:c.589-38C>T MANE Select NP_036469.2:n.589-38C>T