Canonical Allele Identifier: CA903358511
Gene: CCDC39 HGNC NCBI

Linked Data

dbSNP Id: rs1393578023
MyVariant Identifiers: chr3:g.180377816A>T (hg19) chr3:g.180660028A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180660028A>T , CM000665.2:g.180660028A>T GRCh38
NC_000003.11:g.180377816A>T , CM000665.1:g.180377816A>T GRCh37
NC_000003.10:g.181860510A>T NCBI36
NG_029581.1:g.24468T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.517-259T>A MANE Select ENSP00000417960.2:n.517-259T>A
ENST00000650641.1:n.596-259T>A
ENST00000650889.1:n.689-259T>A
ENST00000651046.1:c.517-259T>A ENSP00000499175.1:n.517-259T>A
ENST00000651818.1:n.659-259T>A
ENST00000652024.1:n.608-259T>A
ENST00000652408.1:n.654-259T>A
ENST00000442201.6:c.517-259T>A ENSP00000405708.2:n.517-259T>A
ENST00000476379.5:c.517-259T>A ENSP00000417960.1:n.517-259T>A
NM_181426.1:c.517-259T>A NP_852091.1:n.517-259T>A
NM_181426.2:c.517-259T>A MANE Select NP_852091.1:n.517-259T>A
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