Canonical Allele Identifier: CA1718709269
Gene: CCDC146 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.77133463G= , CM000669.2:g.77133463G= GRCh38
NC_000007.13:g.76762780G= , CM000669.1:g.76762780G= GRCh37
NC_000007.12:g.76600716G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000285871.5:c.-12+10731G= MANE Select ENSP00000285871.4:n.-12+10731G=
ENST00000285871.4:c.-12+10731G= ENSP00000285871.4:n.-12+10731G=
ENST00000415750.5:c.-12+10995G= ENSP00000388649.1:n.-12+10995G=
NM_020879.2:c.-12+10731G= NP_065930.2:n.-12+10731G=
XR_927691.1:n.48-4737C=
NM_020879.3:c.-12+10731G= MANE Select NP_065930.2:n.-12+10731G=
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