Canonical Allele Identifier: CA1424310533

Gene: CCDC39

Linked Data

• dbSNP Id: rs1711698712

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659847_180659848del , CM000665.2:g.180659847_180659848del	GRCh38
NC_000003.11:g.180377635_180377636del , CM000665.1:g.180377635_180377636del	GRCh37
NC_000003.10:g.181860329_181860330del	NCBI36
NG_029581.1:g.24649_24650del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.517-78_517-77del MANE Select	ENSP00000417960.2:n.517-78_517-77del
ENST00000650641.1:n.596-78_596-77del
ENST00000650889.1:n.689-78_689-77del
ENST00000651046.1:c.517-78_517-77del	ENSP00000499175.1:n.517-78_517-77del
ENST00000651818.1:n.659-78_659-77del
ENST00000652024.1:n.608-78_608-77del
ENST00000652408.1:n.654-78_654-77del
ENST00000442201.6:c.517-78_517-77del	ENSP00000405708.2:n.517-78_517-77del
ENST00000476379.5:c.517-78_517-77del	ENSP00000417960.1:n.517-78_517-77del
NM_181426.1:c.517-78_517-77del	NP_852091.1:n.517-78_517-77del
NM_181426.2:c.517-78_517-77del MANE Select	NP_852091.1:n.517-78_517-77del