Canonical Allele Identifier: CA1424310378
Gene: CCDC39 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659523_180659526delinsGTTC , CM000665.2:g.180659523_180659526delinsGTTC GRCh38
NC_000003.11:g.180377311_180377314delinsGTTC , CM000665.1:g.180377311_180377314delinsGTTC GRCh37
NC_000003.10:g.181860005_181860008delinsGTTC NCBI36
NG_029581.1:g.24970_24973delinsGAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.664_667delinsGAAC MANE Select ENSP00000417960.2:p.Glu222=
ENST00000650641.1:n.743_746delinsGAAC
ENST00000650889.1:n.836_839delinsGAAC
ENST00000651046.1:c.664_667delinsGAAC ENSP00000499175.1:p.Glu222=
ENST00000651818.1:n.806_809delinsGAAC
ENST00000652024.1:n.755_758delinsGAAC
ENST00000652408.1:n.801_804delinsGAAC
ENST00000442201.6:c.664_667delinsGAAC ENSP00000405708.2:p.Glu222=
ENST00000476379.5:c.664_667delinsGAAC ENSP00000417960.1:p.Glu222=
NM_181426.1:c.664_667delinsGAAC NP_852091.1:p.Glu222=
NM_181426.2:c.664_667delinsGAAC MANE Select NP_852091.1:p.Glu222=
Search 100 bp 5'
Search 100 bp 3'