Canonical Allele Identifier: CA355301899
Gene: CCDC39 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659466C>G , CM000665.2:g.180659466C>G GRCh38
NC_000003.11:g.180377254C>G , CM000665.1:g.180377254C>G GRCh37
NC_000003.10:g.181859948C>G NCBI36
NG_029581.1:g.25030G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.724G>C MANE Select ENSP00000417960.2:p.Asp242His
ENST00000650641.1:n.803G>C
ENST00000650889.1:n.896G>C
ENST00000651046.1:c.724G>C ENSP00000499175.1:p.Asp242His
ENST00000651818.1:n.866G>C
ENST00000652024.1:n.815G>C
ENST00000652408.1:n.861G>C
ENST00000442201.6:c.724G>C ENSP00000405708.2:p.Asp242His
ENST00000476379.5:c.724G>C ENSP00000417960.1:p.Asp242His
NM_181426.1:c.724G>C NP_852091.1:p.Asp242His
NM_181426.2:c.724G>C MANE Select NP_852091.1:p.Asp242His