Canonical Allele Identifier: CA1424310627

Gene: CCDC39

Linked Data

• dbSNP Id: rs1711703929

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180660023_180660024del , CM000665.2:g.180660023_180660024del	GRCh38
NC_000003.11:g.180377811_180377812del , CM000665.1:g.180377811_180377812del	GRCh37
NC_000003.10:g.181860505_181860506del	NCBI36
NG_029581.1:g.24472_24473del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.517-255_517-254del MANE Select	ENSP00000417960.2:n.517-255_517-254del
ENST00000650641.1:n.596-255_596-254del
ENST00000650889.1:n.689-255_689-254del
ENST00000651046.1:c.517-255_517-254del	ENSP00000499175.1:n.517-255_517-254del
ENST00000651818.1:n.659-255_659-254del
ENST00000652024.1:n.608-255_608-254del
ENST00000652408.1:n.654-255_654-254del
ENST00000442201.6:c.517-255_517-254del	ENSP00000405708.2:n.517-255_517-254del
ENST00000476379.5:c.517-255_517-254del	ENSP00000417960.1:n.517-255_517-254del
NM_181426.1:c.517-255_517-254del	NP_852091.1:n.517-255_517-254del
NM_181426.2:c.517-255_517-254del MANE Select	NP_852091.1:n.517-255_517-254del