Canonical Allele Identifier: CA2677539716
Gene: TDP2 HGNC NCBI

Linked Data

gnomAD v4: 6-24658465-T-G

Genomic Alleles

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

Transcript Alleles

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