Canonical Allele Identifier: CA2648611224
Gene: CFAP45 HGNC NCBI

Linked Data

gnomAD v4: 1-159886799-CTGCTCACAAG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886801_159886810del , CM000663.2:g.159886801_159886810del GRCh38
NC_000001.10:g.159856591_159856600del , CM000663.1:g.159856591_159856600del GRCh37
NC_000001.9:g.158123215_158123224del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.589-120_589-111del MANE Select ENSP00000357079.4:n.589-120_589-111del
ENST00000368099.8:c.589-120_589-111del ENSP00000357079.4:n.589-120_589-111del
ENST00000426543.6:c.334-120_334-111del ENSP00000403044.2:n.334-120_334-111del
ENST00000476696.5:c.589-120_589-111del ENSP00000483972.1:n.589-120_589-111del
ENST00000479940.2:c.334-120_334-111del ENSP00000478944.1:n.334-120_334-111del
NM_012337.2:c.589-120_589-111del NP_036469.2:n.589-120_589-111del
NM_012337.3:c.589-120_589-111del MANE Select NP_036469.2:n.589-120_589-111del
Search 100 bp 5'
Search 100 bp 3'