Canonical Allele Identifier: CA1718709265
Gene: CCDC146 HGNC NCBI

Linked Data

dbSNP Id: rs1584014044

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.77133447T>G , CM000669.2:g.77133447T>G GRCh38
NC_000007.13:g.76762764T>G , CM000669.1:g.76762764T>G GRCh37
NC_000007.12:g.76600700T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000285871.5:c.-12+10715T>G MANE Select ENSP00000285871.4:n.-12+10715T>G
ENST00000285871.4:c.-12+10715T>G ENSP00000285871.4:n.-12+10715T>G
ENST00000415750.5:c.-12+10979T>G ENSP00000388649.1:n.-12+10979T>G
NM_020879.2:c.-12+10715T>G NP_065930.2:n.-12+10715T>G
XR_927691.1:n.48-4721A>C
NM_020879.3:c.-12+10715T>G MANE Select NP_065930.2:n.-12+10715T>G