Canonical Allele Identifier: CA1424310492

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659758_180659760delinsCAG , CM000665.2:g.180659758_180659760delinsCAG	GRCh38
NC_000003.11:g.180377546_180377548delinsCAG , CM000665.1:g.180377546_180377548delinsCAG	GRCh37
NC_000003.10:g.181860240_181860242delinsCAG	NCBI36
NG_029581.1:g.24736_24738delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.526_528delinsCTG MANE Select	ENSP00000417960.2:p.Leu176=
ENST00000650641.1:n.605_607delinsCTG
ENST00000650889.1:n.698_700delinsCTG
ENST00000651046.1:c.526_528delinsCTG	ENSP00000499175.1:p.Leu176=
ENST00000651818.1:n.668_670delinsCTG
ENST00000652024.1:n.617_619delinsCTG
ENST00000652408.1:n.663_665delinsCTG
ENST00000442201.6:c.526_528delinsCTG	ENSP00000405708.2:p.Leu176=
ENST00000476379.5:c.526_528delinsCTG	ENSP00000417960.1:p.Leu176=
NM_181426.1:c.526_528delinsCTG	NP_852091.1:p.Leu176=
NM_181426.2:c.526_528delinsCTG MANE Select	NP_852091.1:p.Leu176=