Canonical Allele Identifier: CA1424310361

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659484T= , CM000665.2:g.180659484T=	GRCh38
NC_000003.11:g.180377272T= , CM000665.1:g.180377272T=	GRCh37
NC_000003.10:g.181859966T=	NCBI36
NG_029581.1:g.25012A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.706A= MANE Select	ENSP00000417960.2:p.Lys236=
ENST00000650641.1:n.785A=
ENST00000650889.1:n.878A=
ENST00000651046.1:c.706A=	ENSP00000499175.1:p.Lys236=
ENST00000651818.1:n.848A=
ENST00000652024.1:n.797A=
ENST00000652408.1:n.843A=
ENST00000442201.6:c.706A=	ENSP00000405708.2:p.Lys236=
ENST00000476379.5:c.706A=	ENSP00000417960.1:p.Lys236=
NM_181426.1:c.706A=	NP_852091.1:p.Lys236=
NM_181426.2:c.706A= MANE Select	NP_852091.1:p.Lys236=