Canonical Allele Identifier: CA264593836

Gene: TDP1

Linked Data

• dbSNP Id: rs770452022
• gnomAD v4: 14-90043126-A-T
• MyVariant Identifiers: chr14:g.90509470A>T (hg19) ; chr14:g.90043126A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90043126A>T , CM000676.2:g.90043126A>T	GRCh38
NC_000014.8:g.90509470A>T , CM000676.1:g.90509470A>T	GRCh37
NC_000014.7:g.89579223A>T	NCBI36
NG_009164.1:g.92225A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000335725.9:c.1810A>T MANE Select	ENSP00000337353.4:p.Met604Leu
ENST00000335725.8:c.1810A>T	ENSP00000337353.4:p.Met604Leu
ENST00000393452.7:c.*86A>T	ENSP00000377098.3:n.*86A>T
ENST00000393454.6:c.1810A>T	ENSP00000377099.2:p.Met604Leu
ENST00000545686.6:c.*1133A>T	ENSP00000444587.2:n.*1133A>T
ENST00000554976.5:c.*1369A>T	ENSP00000452042.1:n.*1369A>T
ENST00000555178.5:c.*995A>T	ENSP00000452363.1:n.*995A>T
ENST00000555880.5:c.1701A>T	ENSP00000450628.1:p.Thr567=
NM_001008744.1:c.1810A>T	NP_001008744.1:p.Met604Leu
NM_018319.3:c.1810A>T	NP_060789.2:p.Met604Leu
XM_005267847.2:c.1810A>T	XP_005267904.1:p.Met604Leu
XM_005267848.1:c.1810A>T	XP_005267905.1:p.Met604Leu
XM_006720197.2:c.1810A>T	XP_006720260.1:p.Met604Leu
XM_006720198.2:c.1810A>T	XP_006720261.1:p.Met604Leu
XM_006720199.1:c.1015A>T	XP_006720262.1:p.Met339Leu
XM_006720200.2:c.1015A>T	XP_006720263.1:p.Met339Leu
XM_011536941.1:c.1810A>T	XP_011535243.1:p.Met604Leu
XM_011536942.1:c.1810A>T	XP_011535244.1:p.Met604Leu
XM_011536943.1:c.1810A>T	XP_011535245.1:p.Met604Leu
XM_011536944.1:c.1701A>T	XP_011535246.1:p.Thr567=
NM_001330205.1:c.1701A>T	NP_001317134.1:p.Thr567=
XM_005267848.3:c.1810A>T	XP_005267905.1:p.Met604Leu
XM_006720197.4:c.1810A>T	XP_006720260.1:p.Met604Leu
XM_011536942.3:c.1810A>T	XP_011535244.1:p.Met604Leu
XM_011536944.2:c.1701A>T	XP_011535246.1:p.Thr567=
XM_017021439.2:c.1810A>T	XP_016876928.1:p.Met604Leu
XM_017021440.2:c.1701A>T	XP_016876929.1:p.Thr567=
XM_024449649.1:c.1936A>T	XP_024305417.1:p.Met646Leu
XM_024449650.1:c.1936A>T	XP_024305418.1:p.Met646Leu
XM_024449651.1:c.1936A>T	XP_024305419.1:p.Met646Leu
XM_024449652.1:c.1936A>T	XP_024305420.1:p.Met646Leu
XM_024449653.1:c.1936A>T	XP_024305421.1:p.Met646Leu
XM_024449654.1:c.1936A>T	XP_024305422.1:p.Met646Leu
XM_024449655.1:c.1936A>T	XP_024305423.1:p.Met646Leu
XM_024449656.1:c.1936A>T	XP_024305424.1:p.Met646Leu
XM_024449657.1:c.1093A>T	XP_024305425.1:p.Met365Leu
XM_024449658.1:c.1093A>T	XP_024305426.1:p.Met365Leu
XM_024449659.1:c.984A>T	XP_024305427.1:p.Thr328=
XR_001750427.2:n.2040A>T
XR_943492.3:n.2314A>T
NM_001008744.2:c.1810A>T	NP_001008744.1:p.Met604Leu
NM_001330205.2:c.1701A>T	NP_001317134.1:p.Thr567=
NM_018319.4:c.1810A>T MANE Select	NP_060789.2:p.Met604Leu