Canonical Allele Identifier: CA1424310543
Gene: CCDC39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659859A= , CM000665.2:g.180659859A= GRCh38
NC_000003.11:g.180377647A= , CM000665.1:g.180377647A= GRCh37
NC_000003.10:g.181860341A= NCBI36
NG_029581.1:g.24637T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.517-90T= MANE Select ENSP00000417960.2:n.517-90T=
ENST00000650641.1:n.596-90T=
ENST00000650889.1:n.689-90T=
ENST00000651046.1:c.517-90T= ENSP00000499175.1:n.517-90T=
ENST00000651818.1:n.659-90T=
ENST00000652024.1:n.608-90T=
ENST00000652408.1:n.654-90T=
ENST00000442201.6:c.517-90T= ENSP00000405708.2:n.517-90T=
ENST00000476379.5:c.517-90T= ENSP00000417960.1:n.517-90T=
NM_181426.1:c.517-90T= NP_852091.1:n.517-90T=
NM_181426.2:c.517-90T= MANE Select NP_852091.1:n.517-90T=