Canonical Allele Identifier: CA2668664443
Gene: CCDC39 HGNC NCBI

Linked Data

gnomAD v4: 3-180659803-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659803C>T , CM000665.2:g.180659803C>T GRCh38
NC_000003.11:g.180377591C>T , CM000665.1:g.180377591C>T GRCh37
NC_000003.10:g.181860285C>T NCBI36
NG_029581.1:g.24693G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.517-34G>A MANE Select ENSP00000417960.2:n.517-34G>A
ENST00000650641.1:n.596-34G>A
ENST00000650889.1:n.689-34G>A
ENST00000651046.1:c.517-34G>A ENSP00000499175.1:n.517-34G>A
ENST00000651818.1:n.659-34G>A
ENST00000652024.1:n.608-34G>A
ENST00000652408.1:n.654-34G>A
ENST00000442201.6:c.517-34G>A ENSP00000405708.2:n.517-34G>A
ENST00000476379.5:c.517-34G>A ENSP00000417960.1:n.517-34G>A
NM_181426.1:c.517-34G>A NP_852091.1:n.517-34G>A
NM_181426.2:c.517-34G>A MANE Select NP_852091.1:n.517-34G>A
Search 100 bp 5'
Search 100 bp 3'