Canonical Allele Identifier: CA1424310347

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659466_180659468delinsCTA , CM000665.2:g.180659466_180659468delinsCTA	GRCh38
NC_000003.11:g.180377254_180377256delinsCTA , CM000665.1:g.180377254_180377256delinsCTA	GRCh37
NC_000003.10:g.181859948_181859950delinsCTA	NCBI36
NG_029581.1:g.25028_25030delinsTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.722_724delinsTAG MANE Select	ENSP00000417960.2:p.Ile241=
ENST00000650641.1:n.801_803delinsTAG
ENST00000650889.1:n.894_896delinsTAG
ENST00000651046.1:c.722_724delinsTAG	ENSP00000499175.1:p.Ile241=
ENST00000651818.1:n.864_866delinsTAG
ENST00000652024.1:n.813_815delinsTAG
ENST00000652408.1:n.859_861delinsTAG
ENST00000442201.6:c.722_724delinsTAG	ENSP00000405708.2:p.Ile241=
ENST00000476379.5:c.722_724delinsTAG	ENSP00000417960.1:p.Ile241=
NM_181426.1:c.722_724delinsTAG	NP_852091.1:p.Ile241=
NM_181426.2:c.722_724delinsTAG MANE Select	NP_852091.1:p.Ile241=