Canonical Allele Identifier: CA1424310338

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659440C= , CM000665.2:g.180659440C=	GRCh38
NC_000003.11:g.180377228C= , CM000665.1:g.180377228C=	GRCh37
NC_000003.10:g.181859922C=	NCBI36
NG_029581.1:g.25056G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.738+12G= MANE Select	ENSP00000417960.2:n.738+12G=
ENST00000650641.1:n.817+12G=
ENST00000650889.1:n.910+12G=
ENST00000651046.1:c.738+12G=	ENSP00000499175.1:n.738+12G=
ENST00000651818.1:n.880+12G=
ENST00000652024.1:n.829+12G=
ENST00000652408.1:n.875+12G=
ENST00000442201.6:c.738+12G=	ENSP00000405708.2:n.738+12G=
ENST00000476379.5:c.738+12G=	ENSP00000417960.1:n.738+12G=
NM_181426.1:c.738+12G=	NP_852091.1:n.738+12G=
NM_181426.2:c.738+12G= MANE Select	NP_852091.1:n.738+12G=