Canonical Allele Identifier: CA2704751120

Gene: CCDC39

Linked Data

• dbSNP Id: rs1351662479

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659596C>T , CM000665.2:g.180659596C>T	GRCh38
NC_000003.11:g.180377384C>T , CM000665.1:g.180377384C>T	GRCh37
NC_000003.10:g.181860078C>T	NCBI36
NG_029581.1:g.24900G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.610-16G>A MANE Select	ENSP00000417960.2:n.610-16G>A
ENST00000650641.1:n.689-16G>A
ENST00000650889.1:n.782-16G>A
ENST00000651046.1:c.610-16G>A	ENSP00000499175.1:n.610-16G>A
ENST00000651818.1:n.752-16G>A
ENST00000652024.1:n.701-16G>A
ENST00000652408.1:n.747-16G>A
ENST00000442201.6:c.610-16G>A	ENSP00000405708.2:n.610-16G>A
ENST00000476379.5:c.610-16G>A	ENSP00000417960.1:n.610-16G>A
NM_181426.1:c.610-16G>A	NP_852091.1:n.610-16G>A
NM_181426.2:c.610-16G>A MANE Select	NP_852091.1:n.610-16G>A