Canonical Allele Identifier: CA355302002
Gene: CCDC39 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659489A>C , CM000665.2:g.180659489A>C GRCh38
NC_000003.11:g.180377277A>C , CM000665.1:g.180377277A>C GRCh37
NC_000003.10:g.181859971A>C NCBI36
NG_029581.1:g.25007T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.701T>G MANE Select ENSP00000417960.2:p.Met234Arg
ENST00000650641.1:n.780T>G
ENST00000650889.1:n.873T>G
ENST00000651046.1:c.701T>G ENSP00000499175.1:p.Met234Arg
ENST00000651818.1:n.843T>G
ENST00000652024.1:n.792T>G
ENST00000652408.1:n.838T>G
ENST00000442201.6:c.701T>G ENSP00000405708.2:p.Met234Arg
ENST00000476379.5:c.701T>G ENSP00000417960.1:p.Met234Arg
NM_181426.1:c.701T>G NP_852091.1:p.Met234Arg
NM_181426.2:c.701T>G MANE Select NP_852091.1:p.Met234Arg