Canonical Allele Identifier: CA1616601222
Gene: TDP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24658495A= , CM000668.2:g.24658495A= GRCh38
NC_000006.11:g.24658723A= , CM000668.1:g.24658723A= GRCh37
NC_000006.10:g.24766702A= NCBI36
NG_052787.1:g.13393T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378198.9:c.425+66T= MANE Select ENSP00000367440.4:n.425+66T=
ENST00000341060.3:c.251+66T= ENSP00000345345.3:n.251+66T=
ENST00000378198.8:c.425+66T= ENSP00000367440.4:n.425+66T=
ENST00000478285.1:n.612+66T=
ENST00000478507.1:n.320-5342T=
NM_016614.2:c.425+66T= NP_057698.2:n.425+66T=
XR_926244.1:n.552+66T=
NM_016614.3:c.425+66T= MANE Select NP_057698.2:n.425+66T=
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