Canonical Allele Identifier: CA1718709328
Gene: CCDC146 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.77133584T= , CM000669.2:g.77133584T= GRCh38
NC_000007.13:g.76762901T= , CM000669.1:g.76762901T= GRCh37
NC_000007.12:g.76600837T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000285871.5:c.-12+10852T= MANE Select ENSP00000285871.4:n.-12+10852T=
ENST00000285871.4:c.-12+10852T= ENSP00000285871.4:n.-12+10852T=
ENST00000415750.5:c.-12+11116T= ENSP00000388649.1:n.-12+11116T=
NM_020879.2:c.-12+10852T= NP_065930.2:n.-12+10852T=
XR_927691.1:n.48-4858A=
NM_020879.3:c.-12+10852T= MANE Select NP_065930.2:n.-12+10852T=