Canonical Allele Identifier: CA355302333
Gene: CCDC39 HGNC NCBI

Linked Data

COSMIC: COSM4115531 COSM4115532
MyVariant Identifiers: chr3:g.180377341A>C (hg19) chr3:g.180659553A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659553A>C , CM000665.2:g.180659553A>C GRCh38
NC_000003.11:g.180377341A>C , CM000665.1:g.180377341A>C GRCh37
NC_000003.10:g.181860035A>C NCBI36
NG_029581.1:g.24943T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.637T>G MANE Select ENSP00000417960.2:p.Phe213Val
ENST00000650641.1:n.716T>G
ENST00000650889.1:n.809T>G
ENST00000651046.1:c.637T>G ENSP00000499175.1:p.Phe213Val
ENST00000651818.1:n.779T>G
ENST00000652024.1:n.728T>G
ENST00000652408.1:n.774T>G
ENST00000442201.6:c.637T>G ENSP00000405708.2:p.Phe213Val
ENST00000476379.5:c.637T>G ENSP00000417960.1:p.Phe213Val
NM_181426.1:c.637T>G NP_852091.1:p.Phe213Val
NM_181426.2:c.637T>G MANE Select NP_852091.1:p.Phe213Val
Search 100 bp 5'
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