Canonical Allele Identifier: CA1424310563

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659882_180659883delinsCT , CM000665.2:g.180659882_180659883delinsCT	GRCh38
NC_000003.11:g.180377670_180377671delinsCT , CM000665.1:g.180377670_180377671delinsCT	GRCh37
NC_000003.10:g.181860364_181860365delinsCT	NCBI36
NG_029581.1:g.24613_24614delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.517-114_517-113delinsAG MANE Select	ENSP00000417960.2:n.517-114_517-113delinsAG
ENST00000650641.1:n.596-114_596-113delinsAG
ENST00000650889.1:n.689-114_689-113delinsAG
ENST00000651046.1:c.517-114_517-113delinsAG	ENSP00000499175.1:n.517-114_517-113delinsAG
ENST00000651818.1:n.659-114_659-113delinsAG
ENST00000652024.1:n.608-114_608-113delinsAG
ENST00000652408.1:n.654-114_654-113delinsAG
ENST00000442201.6:c.517-114_517-113delinsAG	ENSP00000405708.2:n.517-114_517-113delinsAG
ENST00000476379.5:c.517-114_517-113delinsAG	ENSP00000417960.1:n.517-114_517-113delinsAG
NM_181426.1:c.517-114_517-113delinsAG	NP_852091.1:n.517-114_517-113delinsAG
NM_181426.2:c.517-114_517-113delinsAG MANE Select	NP_852091.1:n.517-114_517-113delinsAG