Canonical Allele Identifier: CA2517763126

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659441_180659443del , CM000665.2:g.180659441_180659443del	GRCh38
NC_000003.11:g.180377229_180377231del , CM000665.1:g.180377229_180377231del	GRCh37
NC_000003.10:g.181859923_181859925del	NCBI36
NG_029581.1:g.25056_25058del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.738+12_738+14del MANE Select	ENSP00000417960.2:n.738+12_738+14del
ENST00000650641.1:n.817+12_817+14del
ENST00000650889.1:n.910+12_910+14del
ENST00000651046.1:c.738+12_738+14del	ENSP00000499175.1:n.738+12_738+14del
ENST00000651818.1:n.880+12_880+14del
ENST00000652024.1:n.829+12_829+14del
ENST00000652408.1:n.875+12_875+14del
ENST00000442201.6:c.738+12_738+14del	ENSP00000405708.2:n.738+12_738+14del
ENST00000476379.5:c.738+12_738+14del	ENSP00000417960.1:n.738+12_738+14del
NM_181426.1:c.738+12_738+14del	NP_852091.1:n.738+12_738+14del
NM_181426.2:c.738+12_738+14del MANE Select	NP_852091.1:n.738+12_738+14del