Canonical Allele Identifier: CA2577967084

Gene: CCDC39

Linked Data

• ClinVar Variation Id: 2729666
• ClinVar RCV Id: RCV003539153

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659445A>G , CM000665.2:g.180659445A>G	GRCh38
NC_000003.11:g.180377233A>G , CM000665.1:g.180377233A>G	GRCh37
NC_000003.10:g.181859927A>G	NCBI36
NG_029581.1:g.25051T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.738+7T>C MANE Select	ENSP00000417960.2:n.738+7T>C
ENST00000650641.1:n.817+7T>C
ENST00000650889.1:n.910+7T>C
ENST00000651046.1:c.738+7T>C	ENSP00000499175.1:n.738+7T>C
ENST00000651818.1:n.880+7T>C
ENST00000652024.1:n.829+7T>C
ENST00000652408.1:n.875+7T>C
ENST00000442201.6:c.738+7T>C	ENSP00000405708.2:n.738+7T>C
ENST00000476379.5:c.738+7T>C	ENSP00000417960.1:n.738+7T>C
NM_181426.1:c.738+7T>C	NP_852091.1:n.738+7T>C
NM_181426.2:c.738+7T>C MANE Select	NP_852091.1:n.738+7T>C