Canonical Allele Identifier: CA1424310589
Gene: CCDC39 HGNC NCBI

Linked Data

dbSNP Id: rs1711701815
gnomAD v3: 3-180659927-A-G
gnomAD v4: 3-180659927-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659927A>G , CM000665.2:g.180659927A>G GRCh38
NC_000003.11:g.180377715A>G , CM000665.1:g.180377715A>G GRCh37
NC_000003.10:g.181860409A>G NCBI36
NG_029581.1:g.24569T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.517-158T>C MANE Select ENSP00000417960.2:n.517-158T>C
ENST00000650641.1:n.596-158T>C
ENST00000650889.1:n.689-158T>C
ENST00000651046.1:c.517-158T>C ENSP00000499175.1:n.517-158T>C
ENST00000651818.1:n.659-158T>C
ENST00000652024.1:n.608-158T>C
ENST00000652408.1:n.654-158T>C
ENST00000442201.6:c.517-158T>C ENSP00000405708.2:n.517-158T>C
ENST00000476379.5:c.517-158T>C ENSP00000417960.1:n.517-158T>C
NM_181426.1:c.517-158T>C NP_852091.1:n.517-158T>C
NM_181426.2:c.517-158T>C MANE Select NP_852091.1:n.517-158T>C
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