Canonical Allele Identifier: CA1424305962

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180650140T= , CM000665.2:g.180650140T=	GRCh38
NC_000003.11:g.180367928T= , CM000665.1:g.180367928T=	GRCh37
NC_000003.10:g.181850622T=	NCBI36
NG_029581.1:g.34356A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.1167+1261A= MANE Select	ENSP00000417960.2:n.1167+1261A=
ENST00000650641.1:n.1054+1261A=
ENST00000650889.1:n.1558+1261A=
ENST00000651046.1:c.975+1261A=	ENSP00000499175.1:n.975+1261A=
ENST00000651818.1:n.1117+1261A=
ENST00000651922.1:n.492+1261A=
ENST00000652024.1:n.1066+1261A=
ENST00000652408.1:n.1304+1261A=
ENST00000442201.6:c.1167+1261A=	ENSP00000405708.2:n.1167+1261A=
ENST00000476379.5:c.1167+1261A=	ENSP00000417960.1:n.1167+1261A=
NM_181426.1:c.1167+1261A=	NP_852091.1:n.1167+1261A=
NM_181426.2:c.1167+1261A= MANE Select	NP_852091.1:n.1167+1261A=