Canonical Allele Identifier: CA1424310349

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659469_180659470delinsTG , CM000665.2:g.180659469_180659470delinsTG	GRCh38
NC_000003.11:g.180377257_180377258delinsTG , CM000665.1:g.180377257_180377258delinsTG	GRCh37
NC_000003.10:g.181859951_181859952delinsTG	NCBI36
NG_029581.1:g.25026_25027delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.720_721delinsCA MANE Select	ENSP00000417960.2:p.Asp240=
ENST00000650641.1:n.799_800delinsCA
ENST00000650889.1:n.892_893delinsCA
ENST00000651046.1:c.720_721delinsCA	ENSP00000499175.1:p.Asp240=
ENST00000651818.1:n.862_863delinsCA
ENST00000652024.1:n.811_812delinsCA
ENST00000652408.1:n.857_858delinsCA
ENST00000442201.6:c.720_721delinsCA	ENSP00000405708.2:p.Asp240=
ENST00000476379.5:c.720_721delinsCA	ENSP00000417960.1:p.Asp240=
NM_181426.1:c.720_721delinsCA	NP_852091.1:p.Asp240=
NM_181426.2:c.720_721delinsCA MANE Select	NP_852091.1:p.Asp240=