Canonical Allele Identifier: CA1718709279
Gene: CCDC146 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.77133480T= , CM000669.2:g.77133480T= GRCh38
NC_000007.13:g.76762797T= , CM000669.1:g.76762797T= GRCh37
NC_000007.12:g.76600733T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000285871.5:c.-12+10748T= MANE Select ENSP00000285871.4:n.-12+10748T=
ENST00000285871.4:c.-12+10748T= ENSP00000285871.4:n.-12+10748T=
ENST00000415750.5:c.-12+11012T= ENSP00000388649.1:n.-12+11012T=
NM_020879.2:c.-12+10748T= NP_065930.2:n.-12+10748T=
XR_927691.1:n.48-4754A=
NM_020879.3:c.-12+10748T= MANE Select NP_065930.2:n.-12+10748T=