Canonical Allele Identifier: CA2154324000
Gene: TDP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90043016G= , CM000676.2:g.90043016G= GRCh38
NC_000014.8:g.90509360G= , CM000676.1:g.90509360G= GRCh37
NC_000014.7:g.89579113G= NCBI36
NG_009164.1:g.92115G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000335725.9:c.1754-54G= MANE Select ENSP00000337353.4:n.1754-54G=
ENST00000335725.8:c.1754-54G= ENSP00000337353.4:n.1754-54G=
ENST00000393452.7:c.*30-54G= ENSP00000377098.3:n.*30-54G=
ENST00000393454.6:c.1754-54G= ENSP00000377099.2:n.1754-54G=
ENST00000545686.6:c.*1077-54G= ENSP00000444587.2:n.*1077-54G=
ENST00000554976.5:c.*1313-54G= ENSP00000452042.1:n.*1313-54G=
ENST00000555178.5:c.*939-54G= ENSP00000452363.1:n.*939-54G=
ENST00000555880.5:c.1645-54G= ENSP00000450628.1:n.1645-54G=
NM_001008744.1:c.1754-54G= NP_001008744.1:n.1754-54G=
NM_018319.3:c.1754-54G= NP_060789.2:n.1754-54G=
XM_005267847.2:c.1754-54G= XP_005267904.1:n.1754-54G=
XM_005267848.1:c.1754-54G= XP_005267905.1:n.1754-54G=
XM_006720197.2:c.1754-54G= XP_006720260.1:n.1754-54G=
XM_006720198.2:c.1754-54G= XP_006720261.1:n.1754-54G=
XM_006720199.1:c.959-54G= XP_006720262.1:n.959-54G=
XM_006720200.2:c.959-54G= XP_006720263.1:n.959-54G=
XM_011536941.1:c.1754-54G= XP_011535243.1:n.1754-54G=
XM_011536942.1:c.1754-54G= XP_011535244.1:n.1754-54G=
XM_011536943.1:c.1754-54G= XP_011535245.1:n.1754-54G=
XM_011536944.1:c.1645-54G= XP_011535246.1:n.1645-54G=
NM_001330205.1:c.1645-54G= NP_001317134.1:n.1645-54G=
XM_005267848.3:c.1754-54G= XP_005267905.1:n.1754-54G=
XM_006720197.4:c.1754-54G= XP_006720260.1:n.1754-54G=
XM_011536942.3:c.1754-54G= XP_011535244.1:n.1754-54G=
XM_011536944.2:c.1645-54G= XP_011535246.1:n.1645-54G=
XM_017021439.2:c.1754-54G= XP_016876928.1:n.1754-54G=
XM_017021440.2:c.1645-54G= XP_016876929.1:n.1645-54G=
XM_024449649.1:c.1880-54G= XP_024305417.1:n.1880-54G=
XM_024449650.1:c.1880-54G= XP_024305418.1:n.1880-54G=
XM_024449651.1:c.1880-54G= XP_024305419.1:n.1880-54G=
XM_024449652.1:c.1880-54G= XP_024305420.1:n.1880-54G=
XM_024449653.1:c.1880-54G= XP_024305421.1:n.1880-54G=
XM_024449654.1:c.1880-54G= XP_024305422.1:n.1880-54G=
XM_024449655.1:c.1880-54G= XP_024305423.1:n.1880-54G=
XM_024449656.1:c.1880-54G= XP_024305424.1:n.1880-54G=
XM_024449657.1:c.1037-54G= XP_024305425.1:n.1037-54G=
XM_024449658.1:c.1037-54G= XP_024305426.1:n.1037-54G=
XM_024449659.1:c.928-54G= XP_024305427.1:n.928-54G=
XR_001750427.2:n.1984-54G=
XR_943492.3:n.2258-54G=
NM_001008744.2:c.1754-54G= NP_001008744.1:n.1754-54G=
NM_001330205.2:c.1645-54G= NP_001317134.1:n.1645-54G=
NM_018319.4:c.1754-54G= MANE Select NP_060789.2:n.1754-54G=