Canonical Allele Identifier: CA2677539743
Gene: TDP2 HGNC NCBI

Linked Data

gnomAD v4: 6-24658492-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24658492A>G , CM000668.2:g.24658492A>G GRCh38
NC_000006.11:g.24658720A>G , CM000668.1:g.24658720A>G GRCh37
NC_000006.10:g.24766699A>G NCBI36
NG_052787.1:g.13396T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378198.9:c.425+69T>C MANE Select ENSP00000367440.4:n.425+69T>C
ENST00000341060.3:c.251+69T>C ENSP00000345345.3:n.251+69T>C
ENST00000378198.8:c.425+69T>C ENSP00000367440.4:n.425+69T>C
ENST00000478285.1:n.612+69T>C
ENST00000478507.1:n.320-5339T>C
NM_016614.2:c.425+69T>C NP_057698.2:n.425+69T>C
XR_926244.1:n.552+69T>C
NM_016614.3:c.425+69T>C MANE Select NP_057698.2:n.425+69T>C