Canonical Allele Identifier: CA1616601211
Gene: TDP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24658465T= , CM000668.2:g.24658465T= GRCh38
NC_000006.11:g.24658693T= , CM000668.1:g.24658693T= GRCh37
NC_000006.10:g.24766672T= NCBI36
NG_052787.1:g.13423A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378198.9:c.425+96A= MANE Select ENSP00000367440.4:n.425+96A=
ENST00000341060.3:c.251+96A= ENSP00000345345.3:n.251+96A=
ENST00000378198.8:c.425+96A= ENSP00000367440.4:n.425+96A=
ENST00000478285.1:n.612+96A=
ENST00000478507.1:n.320-5312A=
NM_016614.2:c.425+96A= NP_057698.2:n.425+96A=
XR_926244.1:n.552+96A=
NM_016614.3:c.425+96A= MANE Select NP_057698.2:n.425+96A=
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