Canonical Allele Identifier: CA1424310356

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659477_180659479delinsTCC , CM000665.2:g.180659477_180659479delinsTCC	GRCh38
NC_000003.11:g.180377265_180377267delinsTCC , CM000665.1:g.180377265_180377267delinsTCC	GRCh37
NC_000003.10:g.181859959_181859961delinsTCC	NCBI36
NG_029581.1:g.25017_25019delinsGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.711_713delinsGGA MANE Select	ENSP00000417960.2:p.Arg237=
ENST00000650641.1:n.790_792delinsGGA
ENST00000650889.1:n.883_885delinsGGA
ENST00000651046.1:c.711_713delinsGGA	ENSP00000499175.1:p.Arg237=
ENST00000651818.1:n.853_855delinsGGA
ENST00000652024.1:n.802_804delinsGGA
ENST00000652408.1:n.848_850delinsGGA
ENST00000442201.6:c.711_713delinsGGA	ENSP00000405708.2:p.Arg237=
ENST00000476379.5:c.711_713delinsGGA	ENSP00000417960.1:p.Arg237=
NM_181426.1:c.711_713delinsGGA	NP_852091.1:p.Arg237=
NM_181426.2:c.711_713delinsGGA MANE Select	NP_852091.1:p.Arg237=