Canonical Allele Identifier: CA1718709266
Gene: CCDC146 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.77133457T= , CM000669.2:g.77133457T= GRCh38
NC_000007.13:g.76762774T= , CM000669.1:g.76762774T= GRCh37
NC_000007.12:g.76600710T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000285871.5:c.-12+10725T= MANE Select ENSP00000285871.4:n.-12+10725T=
ENST00000285871.4:c.-12+10725T= ENSP00000285871.4:n.-12+10725T=
ENST00000415750.5:c.-12+10989T= ENSP00000388649.1:n.-12+10989T=
NM_020879.2:c.-12+10725T= NP_065930.2:n.-12+10725T=
XR_927691.1:n.48-4731A=
NM_020879.3:c.-12+10725T= MANE Select NP_065930.2:n.-12+10725T=
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