Canonical Allele Identifier: CA1616601213
Gene: TDP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24658467G= , CM000668.2:g.24658467G= GRCh38
NC_000006.11:g.24658695G= , CM000668.1:g.24658695G= GRCh37
NC_000006.10:g.24766674G= NCBI36
NG_052787.1:g.13421C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378198.9:c.425+94C= MANE Select ENSP00000367440.4:n.425+94C=
ENST00000341060.3:c.251+94C= ENSP00000345345.3:n.251+94C=
ENST00000378198.8:c.425+94C= ENSP00000367440.4:n.425+94C=
ENST00000478285.1:n.612+94C=
ENST00000478507.1:n.320-5314C=
NM_016614.2:c.425+94C= NP_057698.2:n.425+94C=
XR_926244.1:n.552+94C=
NM_016614.3:c.425+94C= MANE Select NP_057698.2:n.425+94C=
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