Canonical Allele Identifier: CA355302166
Gene: CCDC39 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659520T>A , CM000665.2:g.180659520T>A GRCh38
NC_000003.11:g.180377308T>A , CM000665.1:g.180377308T>A GRCh37
NC_000003.10:g.181860002T>A NCBI36
NG_029581.1:g.24976A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.670A>T MANE Select ENSP00000417960.2:p.Ile224Phe
ENST00000650641.1:n.749A>T
ENST00000650889.1:n.842A>T
ENST00000651046.1:c.670A>T ENSP00000499175.1:p.Ile224Phe
ENST00000651818.1:n.812A>T
ENST00000652024.1:n.761A>T
ENST00000652408.1:n.807A>T
ENST00000442201.6:c.670A>T ENSP00000405708.2:p.Ile224Phe
ENST00000476379.5:c.670A>T ENSP00000417960.1:p.Ile224Phe
NM_181426.1:c.670A>T NP_852091.1:p.Ile224Phe
NM_181426.2:c.670A>T MANE Select NP_852091.1:p.Ile224Phe