Canonical Allele Identifier: CA842429938
Gene: CCDC146 HGNC NCBI

Linked Data

dbSNP Id: rs1245017803

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.77133469del , CM000669.2:g.77133469del GRCh38
NC_000007.13:g.76762786del , CM000669.1:g.76762786del GRCh37
NC_000007.12:g.76600722del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000285871.5:c.-12+10737del MANE Select ENSP00000285871.4:n.-12+10737del
ENST00000285871.4:c.-12+10737del ENSP00000285871.4:n.-12+10737del
ENST00000415750.5:c.-12+11001del ENSP00000388649.1:n.-12+11001del
NM_020879.2:c.-12+10737del NP_065930.2:n.-12+10737del
XR_927691.1:n.48-4743del
NM_020879.3:c.-12+10737del MANE Select NP_065930.2:n.-12+10737del