Canonical Allele Identifier: CA1718709302
Gene: CCDC146 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.77133536G= , CM000669.2:g.77133536G= GRCh38
NC_000007.13:g.76762853G= , CM000669.1:g.76762853G= GRCh37
NC_000007.12:g.76600789G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000285871.5:c.-12+10804G= MANE Select ENSP00000285871.4:n.-12+10804G=
ENST00000285871.4:c.-12+10804G= ENSP00000285871.4:n.-12+10804G=
ENST00000415750.5:c.-12+11068G= ENSP00000388649.1:n.-12+11068G=
NM_020879.2:c.-12+10804G= NP_065930.2:n.-12+10804G=
XR_927691.1:n.48-4810C=
NM_020879.3:c.-12+10804G= MANE Select NP_065930.2:n.-12+10804G=