Canonical Allele Identifier: CA390584518

Gene: TDP1

Linked Data

• MyVariant Identifiers: chr14:g.90509459C>A (hg19) ; chr14:g.90043115C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90043115C>A , CM000676.2:g.90043115C>A	GRCh38
NC_000014.8:g.90509459C>A , CM000676.1:g.90509459C>A	GRCh37
NC_000014.7:g.89579212C>A	NCBI36
NG_009164.1:g.92214C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000335725.9:c.1799C>A MANE Select	ENSP00000337353.4:p.Thr600Lys
ENST00000335725.8:c.1799C>A	ENSP00000337353.4:p.Thr600Lys
ENST00000393452.7:c.*75C>A	ENSP00000377098.3:n.*75C>A
ENST00000393454.6:c.1799C>A	ENSP00000377099.2:p.Thr600Lys
ENST00000545686.6:c.*1122C>A	ENSP00000444587.2:n.*1122C>A
ENST00000554976.5:c.*1358C>A	ENSP00000452042.1:n.*1358C>A
ENST00000555178.5:c.*984C>A	ENSP00000452363.1:n.*984C>A
ENST00000555880.5:c.1690C>A	ENSP00000450628.1:p.Arg564Ser
NM_001008744.1:c.1799C>A	NP_001008744.1:p.Thr600Lys
NM_018319.3:c.1799C>A	NP_060789.2:p.Thr600Lys
XM_005267847.2:c.1799C>A	XP_005267904.1:p.Thr600Lys
XM_005267848.1:c.1799C>A	XP_005267905.1:p.Thr600Lys
XM_006720197.2:c.1799C>A	XP_006720260.1:p.Thr600Lys
XM_006720198.2:c.1799C>A	XP_006720261.1:p.Thr600Lys
XM_006720199.1:c.1004C>A	XP_006720262.1:p.Thr335Lys
XM_006720200.2:c.1004C>A	XP_006720263.1:p.Thr335Lys
XM_011536941.1:c.1799C>A	XP_011535243.1:p.Thr600Lys
XM_011536942.1:c.1799C>A	XP_011535244.1:p.Thr600Lys
XM_011536943.1:c.1799C>A	XP_011535245.1:p.Thr600Lys
XM_011536944.1:c.1690C>A	XP_011535246.1:p.Arg564Ser
NM_001330205.1:c.1690C>A	NP_001317134.1:p.Arg564Ser
XM_005267848.3:c.1799C>A	XP_005267905.1:p.Thr600Lys
XM_006720197.4:c.1799C>A	XP_006720260.1:p.Thr600Lys
XM_011536942.3:c.1799C>A	XP_011535244.1:p.Thr600Lys
XM_011536944.2:c.1690C>A	XP_011535246.1:p.Arg564Ser
XM_017021439.2:c.1799C>A	XP_016876928.1:p.Thr600Lys
XM_017021440.2:c.1690C>A	XP_016876929.1:p.Arg564Ser
XM_024449649.1:c.1925C>A	XP_024305417.1:p.Thr642Lys
XM_024449650.1:c.1925C>A	XP_024305418.1:p.Thr642Lys
XM_024449651.1:c.1925C>A	XP_024305419.1:p.Thr642Lys
XM_024449652.1:c.1925C>A	XP_024305420.1:p.Thr642Lys
XM_024449653.1:c.1925C>A	XP_024305421.1:p.Thr642Lys
XM_024449654.1:c.1925C>A	XP_024305422.1:p.Thr642Lys
XM_024449655.1:c.1925C>A	XP_024305423.1:p.Thr642Lys
XM_024449656.1:c.1925C>A	XP_024305424.1:p.Thr642Lys
XM_024449657.1:c.1082C>A	XP_024305425.1:p.Thr361Lys
XM_024449658.1:c.1082C>A	XP_024305426.1:p.Thr361Lys
XM_024449659.1:c.973C>A	XP_024305427.1:p.Arg325Ser
XR_001750427.2:n.2029C>A
XR_943492.3:n.2303C>A
NM_001008744.2:c.1799C>A	NP_001008744.1:p.Thr600Lys
NM_001330205.2:c.1690C>A	NP_001317134.1:p.Arg564Ser
NM_018319.4:c.1799C>A MANE Select	NP_060789.2:p.Thr600Lys