Canonical Allele Identifier: CA1424310360

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659483T= , CM000665.2:g.180659483T=	GRCh38
NC_000003.11:g.180377271T= , CM000665.1:g.180377271T=	GRCh37
NC_000003.10:g.181859965T=	NCBI36
NG_029581.1:g.25013A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.707A= MANE Select	ENSP00000417960.2:p.Lys236=
ENST00000650641.1:n.786A=
ENST00000650889.1:n.879A=
ENST00000651046.1:c.707A=	ENSP00000499175.1:p.Lys236=
ENST00000651818.1:n.849A=
ENST00000652024.1:n.798A=
ENST00000652408.1:n.844A=
ENST00000442201.6:c.707A=	ENSP00000405708.2:p.Lys236=
ENST00000476379.5:c.707A=	ENSP00000417960.1:p.Lys236=
NM_181426.1:c.707A=	NP_852091.1:p.Lys236=
NM_181426.2:c.707A= MANE Select	NP_852091.1:p.Lys236=