Canonical Allele Identifier: CA355301968
Gene: CCDC39 HGNC NCBI

Linked Data

dbSNP Id: rs1347216428

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659480C>T , CM000665.2:g.180659480C>T GRCh38
NC_000003.11:g.180377268C>T , CM000665.1:g.180377268C>T GRCh37
NC_000003.10:g.181859962C>T NCBI36
NG_029581.1:g.25016G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.710G>A MANE Select ENSP00000417960.2:p.Arg237Lys
ENST00000650641.1:n.789G>A
ENST00000650889.1:n.882G>A
ENST00000651046.1:c.710G>A ENSP00000499175.1:p.Arg237Lys
ENST00000651818.1:n.852G>A
ENST00000652024.1:n.801G>A
ENST00000652408.1:n.847G>A
ENST00000442201.6:c.710G>A ENSP00000405708.2:p.Arg237Lys
ENST00000476379.5:c.710G>A ENSP00000417960.1:p.Arg237Lys
NM_181426.1:c.710G>A NP_852091.1:p.Arg237Lys
NM_181426.2:c.710G>A MANE Select NP_852091.1:p.Arg237Lys