Canonical Allele Identifier: CA2715908

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180644119C>T , CM000665.2:g.180644119C>T	GRCh38
NC_000003.11:g.180361907C>T , CM000665.1:g.180361907C>T	GRCh37
NC_000003.10:g.181844601C>T	NCBI36
NG_029581.1:g.40377G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_181426.2:c.1665+1G>A MANE Select	NP_852091.1:n.1665+1G>A
ENST00000476379.6:c.1665+1G>A MANE Select	ENSP00000417960.2:n.1665+1G>A
NM_181426.1:c.1665+1G>A	NP_852091.1:n.1665+1G>A
ENST00000442201.6:c.1665+1G>A	ENSP00000405708.2:n.1665+1G>A
ENST00000476379.5:c.1665+1G>A	ENSP00000417960.1:n.1665+1G>A
ENST00000650641.1:n.1552+1G>A
ENST00000650889.1:n.4878G>A
ENST00000651046.1:c.1473+1G>A	ENSP00000499175.1:n.1473+1G>A
ENST00000651818.1:n.1616G>A
ENST00000651922.1:n.990+1G>A
ENST00000652408.1:n.1802+1G>A