Canonical Allele Identifier: CA1424310570
Gene: CCDC39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659896_180659900delinsTAATA , CM000665.2:g.180659896_180659900delinsTAATA GRCh38
NC_000003.11:g.180377684_180377688delinsTAATA , CM000665.1:g.180377684_180377688delinsTAATA GRCh37
NC_000003.10:g.181860378_181860382delinsTAATA NCBI36
NG_029581.1:g.24596_24600delinsTATTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.517-131_517-127delinsTATTA MANE Select ENSP00000417960.2:n.517-131_517-127delinsTATTA
ENST00000650641.1:n.596-131_596-127delinsTATTA
ENST00000650889.1:n.689-131_689-127delinsTATTA
ENST00000651046.1:c.517-131_517-127delinsTATTA ENSP00000499175.1:n.517-131_517-127delinsTATTA
ENST00000651818.1:n.659-131_659-127delinsTATTA
ENST00000652024.1:n.608-131_608-127delinsTATTA
ENST00000652408.1:n.654-131_654-127delinsTATTA
ENST00000442201.6:c.517-131_517-127delinsTATTA ENSP00000405708.2:n.517-131_517-127delinsTATTA
ENST00000476379.5:c.517-131_517-127delinsTATTA ENSP00000417960.1:n.517-131_517-127delinsTATTA
NM_181426.1:c.517-131_517-127delinsTATTA NP_852091.1:n.517-131_517-127delinsTATTA
NM_181426.2:c.517-131_517-127delinsTATTA MANE Select NP_852091.1:n.517-131_517-127delinsTATTA