Canonical Allele Identifier: CA136165215
Gene: TDP2 HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24658843A>T , CM000668.2:g.24658843A>T GRCh38
NC_000006.11:g.24659071A>T , CM000668.1:g.24659071A>T GRCh37
NC_000006.10:g.24767050A>T NCBI36
NG_052787.1:g.13045T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378198.9:c.252-109T>A MANE Select ENSP00000367440.4:n.252-109T>A
ENST00000341060.3:c.78-109T>A ENSP00000345345.3:n.78-109T>A
ENST00000378198.8:c.252-109T>A ENSP00000367440.4:n.252-109T>A
ENST00000478285.1:n.330T>A
ENST00000478507.1:n.320-5690T>A
NM_016614.2:c.252-109T>A NP_057698.2:n.252-109T>A
XR_926244.1:n.379-109T>A
NM_016614.3:c.252-109T>A MANE Select NP_057698.2:n.252-109T>A