Canonical Allele Identifier: CA2830543232
Gene: CCDC146 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.77293265del , CM000669.2:g.77293265del GRCh38
NC_000007.13:g.76922582del , CM000669.1:g.76922582del GRCh37
NC_000007.12:g.76760518del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000285871.5:c.2664+65del MANE Select ENSP00000285871.4:n.2664+65del
ENST00000285871.4:c.2664+65del ENSP00000285871.4:n.2664+65del
ENST00000415740.6:n.1851+65del
ENST00000461259.5:n.1003+65del
ENST00000478101.1:n.473+65del
ENST00000488998.1:n.148+65del
NM_020879.2:c.2664+65del NP_065930.2:n.2664+65del
NM_020879.3:c.2664+65del MANE Select NP_065930.2:n.2664+65del