Canonical Allele Identifier: CA355298517

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180651400C>T , CM000665.2:g.180651400C>T	GRCh38
NC_000003.11:g.180369188C>T , CM000665.1:g.180369188C>T	GRCh37
NC_000003.10:g.181851882C>T	NCBI36
NG_029581.1:g.33096G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_181426.2:c.1167+1G>A MANE Select	NP_852091.1:n.1167+1G>A
ENST00000476379.6:c.1167+1G>A MANE Select	ENSP00000417960.2:n.1167+1G>A
NM_181426.1:c.1167+1G>A	NP_852091.1:n.1167+1G>A
ENST00000442201.6:c.1167+1G>A	ENSP00000405708.2:n.1167+1G>A
ENST00000476379.5:c.1167+1G>A	ENSP00000417960.1:n.1167+1G>A
ENST00000650641.1:n.1054+1G>A
ENST00000650889.1:n.1558+1G>A
ENST00000651046.1:c.975+1G>A	ENSP00000499175.1:n.975+1G>A
ENST00000651818.1:n.1117+1G>A
ENST00000651922.1:n.492+1G>A
ENST00000652024.1:n.1066+1G>A
ENST00000652408.1:n.1304+1G>A