Canonical Allele Identifier: CA355301975
Gene: CCDC39 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659482C>G , CM000665.2:g.180659482C>G GRCh38
NC_000003.11:g.180377270C>G , CM000665.1:g.180377270C>G GRCh37
NC_000003.10:g.181859964C>G NCBI36
NG_029581.1:g.25014G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.708G>C MANE Select ENSP00000417960.2:p.Lys236Asn
ENST00000650641.1:n.787G>C
ENST00000650889.1:n.880G>C
ENST00000651046.1:c.708G>C ENSP00000499175.1:p.Lys236Asn
ENST00000651818.1:n.850G>C
ENST00000652024.1:n.799G>C
ENST00000652408.1:n.845G>C
ENST00000442201.6:c.708G>C ENSP00000405708.2:p.Lys236Asn
ENST00000476379.5:c.708G>C ENSP00000417960.1:p.Lys236Asn
NM_181426.1:c.708G>C NP_852091.1:p.Lys236Asn
NM_181426.2:c.708G>C MANE Select NP_852091.1:p.Lys236Asn