Canonical Allele Identifier: CA2716261

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180679315_180679317del , CM000665.2:g.180679315_180679317del	GRCh38
NC_000003.11:g.180397103_180397105del , CM000665.1:g.180397103_180397105del	GRCh37
NC_000003.10:g.181879797_181879799del	NCBI36
NG_029581.1:g.5182_5184del

Transcript Alleles

HGVS	Amino-acid Change
NM_181426.2:c.67_69del MANE Select	NP_852091.1:p.Glu23del
ENST00000476379.6:c.67_69del MANE Select	ENSP00000417960.2:p.Glu23del
NM_181426.1:c.67_69del	NP_852091.1:p.Glu23del
ENST00000442201.6:c.67_69del	ENSP00000405708.2:p.Glu23del
ENST00000471307.6:c.37-15328_37-15326del	ENSP00000418702.2:n.37-15328_37-15326del
ENST00000476379.5:c.67_69del	ENSP00000417960.1:p.Glu23del
ENST00000650641.1:n.146_148del
ENST00000650889.1:n.262+294_262+296del
ENST00000651046.1:c.67_69del	ENSP00000499175.1:p.Glu23del
ENST00000651818.1:n.232+294_232+296del
ENST00000652024.1:n.158_160del
ENST00000652408.1:n.227+294_227+296del