Canonical Allele Identifier: CA1424310337

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659439A= , CM000665.2:g.180659439A=	GRCh38
NC_000003.11:g.180377227A= , CM000665.1:g.180377227A=	GRCh37
NC_000003.10:g.181859921A=	NCBI36
NG_029581.1:g.25057T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.738+13T= MANE Select	ENSP00000417960.2:n.738+13T=
ENST00000650641.1:n.817+13T=
ENST00000650889.1:n.910+13T=
ENST00000651046.1:c.738+13T=	ENSP00000499175.1:n.738+13T=
ENST00000651818.1:n.880+13T=
ENST00000652024.1:n.829+13T=
ENST00000652408.1:n.875+13T=
ENST00000442201.6:c.738+13T=	ENSP00000405708.2:n.738+13T=
ENST00000476379.5:c.738+13T=	ENSP00000417960.1:n.738+13T=
NM_181426.1:c.738+13T=	NP_852091.1:n.738+13T=
NM_181426.2:c.738+13T= MANE Select	NP_852091.1:n.738+13T=