Canonical Allele Identifier: CA1718709274
Gene: CCDC146 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.77133468A= , CM000669.2:g.77133468A= GRCh38
NC_000007.13:g.76762785A= , CM000669.1:g.76762785A= GRCh37
NC_000007.12:g.76600721A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000285871.5:c.-12+10736A= MANE Select ENSP00000285871.4:n.-12+10736A=
ENST00000285871.4:c.-12+10736A= ENSP00000285871.4:n.-12+10736A=
ENST00000415750.5:c.-12+11000A= ENSP00000388649.1:n.-12+11000A=
NM_020879.2:c.-12+10736A= NP_065930.2:n.-12+10736A=
XR_927691.1:n.48-4742T=
NM_020879.3:c.-12+10736A= MANE Select NP_065930.2:n.-12+10736A=
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