Canonical Allele Identifier: CA1424310575
Gene: CCDC39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659907_180659910delinsTTTC , CM000665.2:g.180659907_180659910delinsTTTC GRCh38
NC_000003.11:g.180377695_180377698delinsTTTC , CM000665.1:g.180377695_180377698delinsTTTC GRCh37
NC_000003.10:g.181860389_181860392delinsTTTC NCBI36
NG_029581.1:g.24586_24589delinsGAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.517-141_517-138delinsGAAA MANE Select ENSP00000417960.2:n.517-141_517-138delinsGAAA
ENST00000650641.1:n.596-141_596-138delinsGAAA
ENST00000650889.1:n.689-141_689-138delinsGAAA
ENST00000651046.1:c.517-141_517-138delinsGAAA ENSP00000499175.1:n.517-141_517-138delinsGAAA
ENST00000651818.1:n.659-141_659-138delinsGAAA
ENST00000652024.1:n.608-141_608-138delinsGAAA
ENST00000652408.1:n.654-141_654-138delinsGAAA
ENST00000442201.6:c.517-141_517-138delinsGAAA ENSP00000405708.2:n.517-141_517-138delinsGAAA
ENST00000476379.5:c.517-141_517-138delinsGAAA ENSP00000417960.1:n.517-141_517-138delinsGAAA
NM_181426.1:c.517-141_517-138delinsGAAA NP_852091.1:n.517-141_517-138delinsGAAA
NM_181426.2:c.517-141_517-138delinsGAAA MANE Select NP_852091.1:n.517-141_517-138delinsGAAA