Canonical Allele Identifier: CA7304119

Gene: TDP1

Linked Data

• dbSNP Id: rs765381161
• ExAC: 14:90509380 CAAAT / C
• gnomAD v2: 14-90509380-CAAAT-C
• gnomAD v3: 14-90043036-CAAAT-C
• gnomAD v4: 14-90043036-CAAAT-C
• MyVariant Identifiers: chr14:g.90509381_90509384del (hg19) ; chr14:g.90043037_90043040del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90043042_90043045del , CM000676.2:g.90043042_90043045del	GRCh38
NC_000014.8:g.90509386_90509389del , CM000676.1:g.90509386_90509389del	GRCh37
NC_000014.7:g.89579139_89579142del	NCBI36
NG_009164.1:g.92141_92144del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335725.9:c.1754-28_1754-25del MANE Select	ENSP00000337353.4:n.1754-28_1754-25del
ENST00000335725.8:c.1754-28_1754-25del	ENSP00000337353.4:n.1754-28_1754-25del
ENST00000393452.7:c.*30-28_*30-25del	ENSP00000377098.3:n.*30-28_*30-25del
ENST00000393454.6:c.1754-28_1754-25del	ENSP00000377099.2:n.1754-28_1754-25del
ENST00000545686.6:c.*1077-28_*1077-25del	ENSP00000444587.2:n.*1077-28_*1077-25del
ENST00000554976.5:c.*1313-28_*1313-25del	ENSP00000452042.1:n.*1313-28_*1313-25del
ENST00000555178.5:c.*939-28_*939-25del	ENSP00000452363.1:n.*939-28_*939-25del
ENST00000555880.5:c.1645-28_1645-25del	ENSP00000450628.1:n.1645-28_1645-25del
NM_001008744.1:c.1754-28_1754-25del	NP_001008744.1:n.1754-28_1754-25del
NM_018319.3:c.1754-28_1754-25del	NP_060789.2:n.1754-28_1754-25del
XM_005267847.2:c.1754-28_1754-25del	XP_005267904.1:n.1754-28_1754-25del
XM_005267848.1:c.1754-28_1754-25del	XP_005267905.1:n.1754-28_1754-25del
XM_006720197.2:c.1754-28_1754-25del	XP_006720260.1:n.1754-28_1754-25del
XM_006720198.2:c.1754-28_1754-25del	XP_006720261.1:n.1754-28_1754-25del
XM_006720199.1:c.959-28_959-25del	XP_006720262.1:n.959-28_959-25del
XM_006720200.2:c.959-28_959-25del	XP_006720263.1:n.959-28_959-25del
XM_011536941.1:c.1754-28_1754-25del	XP_011535243.1:n.1754-28_1754-25del
XM_011536942.1:c.1754-28_1754-25del	XP_011535244.1:n.1754-28_1754-25del
XM_011536943.1:c.1754-28_1754-25del	XP_011535245.1:n.1754-28_1754-25del
XM_011536944.1:c.1645-28_1645-25del	XP_011535246.1:n.1645-28_1645-25del
NM_001330205.1:c.1645-28_1645-25del	NP_001317134.1:n.1645-28_1645-25del
XM_005267848.3:c.1754-28_1754-25del	XP_005267905.1:n.1754-28_1754-25del
XM_006720197.4:c.1754-28_1754-25del	XP_006720260.1:n.1754-28_1754-25del
XM_011536942.3:c.1754-28_1754-25del	XP_011535244.1:n.1754-28_1754-25del
XM_011536944.2:c.1645-28_1645-25del	XP_011535246.1:n.1645-28_1645-25del
XM_017021439.2:c.1754-28_1754-25del	XP_016876928.1:n.1754-28_1754-25del
XM_017021440.2:c.1645-28_1645-25del	XP_016876929.1:n.1645-28_1645-25del
XM_024449649.1:c.1880-28_1880-25del	XP_024305417.1:n.1880-28_1880-25del
XM_024449650.1:c.1880-28_1880-25del	XP_024305418.1:n.1880-28_1880-25del
XM_024449651.1:c.1880-28_1880-25del	XP_024305419.1:n.1880-28_1880-25del
XM_024449652.1:c.1880-28_1880-25del	XP_024305420.1:n.1880-28_1880-25del
XM_024449653.1:c.1880-28_1880-25del	XP_024305421.1:n.1880-28_1880-25del
XM_024449654.1:c.1880-28_1880-25del	XP_024305422.1:n.1880-28_1880-25del
XM_024449655.1:c.1880-28_1880-25del	XP_024305423.1:n.1880-28_1880-25del
XM_024449656.1:c.1880-28_1880-25del	XP_024305424.1:n.1880-28_1880-25del
XM_024449657.1:c.1037-28_1037-25del	XP_024305425.1:n.1037-28_1037-25del
XM_024449658.1:c.1037-28_1037-25del	XP_024305426.1:n.1037-28_1037-25del
XM_024449659.1:c.928-28_928-25del	XP_024305427.1:n.928-28_928-25del
XR_001750427.2:n.1984-28_1984-25del
XR_943492.3:n.2258-28_2258-25del
NM_001008744.2:c.1754-28_1754-25del	NP_001008744.1:n.1754-28_1754-25del
NM_001330205.2:c.1645-28_1645-25del	NP_001317134.1:n.1645-28_1645-25del
NM_018319.4:c.1754-28_1754-25del MANE Select	NP_060789.2:n.1754-28_1754-25del