Canonical Allele Identifier: CA1424310402
Gene: CCDC39 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659562_180659563delinsCT , CM000665.2:g.180659562_180659563delinsCT GRCh38
NC_000003.11:g.180377350_180377351delinsCT , CM000665.1:g.180377350_180377351delinsCT GRCh37
NC_000003.10:g.181860044_181860045delinsCT NCBI36
NG_029581.1:g.24933_24934delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.627_628delinsAG MANE Select ENSP00000417960.2:p.Ala209=
ENST00000650641.1:n.706_707delinsAG
ENST00000650889.1:n.799_800delinsAG
ENST00000651046.1:c.627_628delinsAG ENSP00000499175.1:p.Ala209=
ENST00000651818.1:n.769_770delinsAG
ENST00000652024.1:n.718_719delinsAG
ENST00000652408.1:n.764_765delinsAG
ENST00000442201.6:c.627_628delinsAG ENSP00000405708.2:p.Ala209=
ENST00000476379.5:c.627_628delinsAG ENSP00000417960.1:p.Ala209=
NM_181426.1:c.627_628delinsAG NP_852091.1:p.Ala209=
NM_181426.2:c.627_628delinsAG MANE Select NP_852091.1:p.Ala209=
Search 100 bp 5'
Search 100 bp 3'