Canonical Allele Identifier: CA1424310397

Gene: CCDC39

Linked Data

• dbSNP Id: rs1711688328

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659556del , CM000665.2:g.180659556del	GRCh38
NC_000003.11:g.180377344del , CM000665.1:g.180377344del	GRCh37
NC_000003.10:g.181860038del	NCBI36
NG_029581.1:g.24940del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.634del MANE Select	ENSP00000417960.2:p.Asp212IlefsTer20
ENST00000650641.1:n.713del
ENST00000650889.1:n.806del
ENST00000651046.1:c.634del	ENSP00000499175.1:p.Asp212IlefsTer20
ENST00000651818.1:n.776del
ENST00000652024.1:n.725del
ENST00000652408.1:n.771del
ENST00000442201.6:c.634del	ENSP00000405708.2:p.Asp212IlefsTer20
ENST00000476379.5:c.634del	ENSP00000417960.1:p.Asp212IlefsTer20
NM_181426.1:c.634del	NP_852091.1:p.Asp212IlefsTer20
NM_181426.2:c.634del MANE Select	NP_852091.1:p.Asp212IlefsTer20