Canonical Allele Identifier: CA1424310612
Gene: CCDC39 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659991T= , CM000665.2:g.180659991T= GRCh38
NC_000003.11:g.180377779T= , CM000665.1:g.180377779T= GRCh37
NC_000003.10:g.181860473T= NCBI36
NG_029581.1:g.24505A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.517-222A= MANE Select ENSP00000417960.2:n.517-222A=
ENST00000650641.1:n.596-222A=
ENST00000650889.1:n.689-222A=
ENST00000651046.1:c.517-222A= ENSP00000499175.1:n.517-222A=
ENST00000651818.1:n.659-222A=
ENST00000652024.1:n.608-222A=
ENST00000652408.1:n.654-222A=
ENST00000442201.6:c.517-222A= ENSP00000405708.2:n.517-222A=
ENST00000476379.5:c.517-222A= ENSP00000417960.1:n.517-222A=
NM_181426.1:c.517-222A= NP_852091.1:n.517-222A=
NM_181426.2:c.517-222A= MANE Select NP_852091.1:n.517-222A=
Search 100 bp 5'
Search 100 bp 3'