Canonical Allele Identifier: CA437079814

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180651401C>T , CM000665.2:g.180651401C>T	GRCh38
NC_000003.11:g.180369189C>T , CM000665.1:g.180369189C>T	GRCh37
NC_000003.10:g.181851883C>T	NCBI36
NG_029581.1:g.33095G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_181426.2:c.1167G>A MANE Select	NP_852091.1:p.Lys389=
ENST00000476379.6:c.1167G>A MANE Select	ENSP00000417960.2:p.Lys389=
NM_181426.1:c.1167G>A	NP_852091.1:p.Lys389=
ENST00000442201.6:c.1167G>A	ENSP00000405708.2:p.Lys389=
ENST00000476379.5:c.1167G>A	ENSP00000417960.1:p.Lys389=
ENST00000650641.1:n.1054G>A
ENST00000650889.1:n.1558G>A
ENST00000651046.1:c.975G>A	ENSP00000499175.1:p.Lys325=
ENST00000651818.1:n.1117G>A
ENST00000651922.1:n.492G>A
ENST00000652024.1:n.1066G>A
ENST00000652408.1:n.1304G>A