Canonical Allele Identifier: CA2586973201
Gene: CCDC39 HGNC NCBI

Linked Data

gnomAD v4: 3-180659456-GCA-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659459_180659460del , CM000665.2:g.180659459_180659460del GRCh38
NC_000003.11:g.180377247_180377248del , CM000665.1:g.180377247_180377248del GRCh37
NC_000003.10:g.181859941_181859942del NCBI36
NG_029581.1:g.25038_25039del

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.732_733del MANE Select ENSP00000417960.2:p.Ala245PhefsTer18
ENST00000650641.1:n.811_812del
ENST00000650889.1:n.904_905del
ENST00000651046.1:c.732_733del ENSP00000499175.1:p.Ala245PhefsTer11
ENST00000651818.1:n.874_875del
ENST00000652024.1:n.823_824del
ENST00000652408.1:n.869_870del
ENST00000442201.6:c.732_733del ENSP00000405708.2:p.Ala245PhefsTer18
ENST00000476379.5:c.732_733del ENSP00000417960.1:p.Ala245PhefsTer18
NM_181426.1:c.732_733del NP_852091.1:p.Ala245PhefsTer18
NM_181426.2:c.732_733del MANE Select NP_852091.1:p.Ala245PhefsTer18
Search 100 bp 5'
Search 100 bp 3'