Canonical Allele Identifier: CA1424310626
Gene: CCDC39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180660022_180660024delinsTAA , CM000665.2:g.180660022_180660024delinsTAA GRCh38
NC_000003.11:g.180377810_180377812delinsTAA , CM000665.1:g.180377810_180377812delinsTAA GRCh37
NC_000003.10:g.181860504_181860506delinsTAA NCBI36
NG_029581.1:g.24472_24474delinsTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.517-255_517-253delinsTTA MANE Select ENSP00000417960.2:n.517-255_517-253delinsTTA
ENST00000650641.1:n.596-255_596-253delinsTTA
ENST00000650889.1:n.689-255_689-253delinsTTA
ENST00000651046.1:c.517-255_517-253delinsTTA ENSP00000499175.1:n.517-255_517-253delinsTTA
ENST00000651818.1:n.659-255_659-253delinsTTA
ENST00000652024.1:n.608-255_608-253delinsTTA
ENST00000652408.1:n.654-255_654-253delinsTTA
ENST00000442201.6:c.517-255_517-253delinsTTA ENSP00000405708.2:n.517-255_517-253delinsTTA
ENST00000476379.5:c.517-255_517-253delinsTTA ENSP00000417960.1:n.517-255_517-253delinsTTA
NM_181426.1:c.517-255_517-253delinsTTA NP_852091.1:n.517-255_517-253delinsTTA
NM_181426.2:c.517-255_517-253delinsTTA MANE Select NP_852091.1:n.517-255_517-253delinsTTA