Canonical Allele Identifier: CA1718709315
Gene: CCDC146 HGNC NCBI

Linked Data

dbSNP Id: rs1790816742

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.77133555T>G , CM000669.2:g.77133555T>G GRCh38
NC_000007.13:g.76762872T>G , CM000669.1:g.76762872T>G GRCh37
NC_000007.12:g.76600808T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000285871.5:c.-12+10823T>G MANE Select ENSP00000285871.4:n.-12+10823T>G
ENST00000285871.4:c.-12+10823T>G ENSP00000285871.4:n.-12+10823T>G
ENST00000415750.5:c.-12+11087T>G ENSP00000388649.1:n.-12+11087T>G
NM_020879.2:c.-12+10823T>G NP_065930.2:n.-12+10823T>G
XR_927691.1:n.48-4829A>C
NM_020879.3:c.-12+10823T>G MANE Select NP_065930.2:n.-12+10823T>G