Canonical Allele Identifier: CA1424310581

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659915C= , CM000665.2:g.180659915C=	GRCh38
NC_000003.11:g.180377703C= , CM000665.1:g.180377703C=	GRCh37
NC_000003.10:g.181860397C=	NCBI36
NG_029581.1:g.24581G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.517-146G= MANE Select	ENSP00000417960.2:n.517-146G=
ENST00000650641.1:n.596-146G=
ENST00000650889.1:n.689-146G=
ENST00000651046.1:c.517-146G=	ENSP00000499175.1:n.517-146G=
ENST00000651818.1:n.659-146G=
ENST00000652024.1:n.608-146G=
ENST00000652408.1:n.654-146G=
ENST00000442201.6:c.517-146G=	ENSP00000405708.2:n.517-146G=
ENST00000476379.5:c.517-146G=	ENSP00000417960.1:n.517-146G=
NM_181426.1:c.517-146G=	NP_852091.1:n.517-146G=
NM_181426.2:c.517-146G= MANE Select	NP_852091.1:n.517-146G=