Canonical Allele Identifier: CA1718709267
Gene: CCDC146 HGNC NCBI

Linked Data

dbSNP Id: rs1790815264

Genomic Alleles

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

Transcript Alleles

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