Canonical Allele Identifier: CA2677539701
Gene: TDP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24658461del , CM000668.2:g.24658461del GRCh38
NC_000006.11:g.24658689del , CM000668.1:g.24658689del GRCh37
NC_000006.10:g.24766668del NCBI36
NG_052787.1:g.13428del

Transcript Alleles

HGVS Amino-acid change
ENST00000378198.9:c.425+101del MANE Select ENSP00000367440.4:n.425+101del
ENST00000341060.3:c.251+101del ENSP00000345345.3:n.251+101del
ENST00000378198.8:c.425+101del ENSP00000367440.4:n.425+101del
ENST00000478285.1:n.612+101del
ENST00000478507.1:n.320-5307del
NM_016614.2:c.425+101del NP_057698.2:n.425+101del
XR_926244.1:n.552+101del
NM_016614.3:c.425+101del MANE Select NP_057698.2:n.425+101del