Canonical Allele Identifier: CA1424310355

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659477T= , CM000665.2:g.180659477T=	GRCh38
NC_000003.11:g.180377265T= , CM000665.1:g.180377265T=	GRCh37
NC_000003.10:g.181859959T=	NCBI36
NG_029581.1:g.25019A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.713A= MANE Select	ENSP00000417960.2:p.Asp238=
ENST00000650641.1:n.792A=
ENST00000650889.1:n.885A=
ENST00000651046.1:c.713A=	ENSP00000499175.1:p.Asp238=
ENST00000651818.1:n.855A=
ENST00000652024.1:n.804A=
ENST00000652408.1:n.850A=
ENST00000442201.6:c.713A=	ENSP00000405708.2:p.Asp238=
ENST00000476379.5:c.713A=	ENSP00000417960.1:p.Asp238=
NM_181426.1:c.713A=	NP_852091.1:p.Asp238=
NM_181426.2:c.713A= MANE Select	NP_852091.1:p.Asp238=