Canonical Allele Identifier: CA10645266

Gene: TDP1

Linked Data

• ClinVar Variation Id: 314853
• ClinVar RCV Id: RCV000343717
• dbSNP Id: rs374734859
• gnomAD v2: 14-90510502-G-A
• gnomAD v3: 14-90044158-G-A
• gnomAD v4: 14-90044158-G-A
• MyVariant Identifiers: chr14:g.90510502G>A (hg19) ; chr14:g.90044158G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90044158G>A , CM000676.2:g.90044158G>A	GRCh38
NC_000014.8:g.90510502G>A , CM000676.1:g.90510502G>A	GRCh37
NC_000014.7:g.89580255G>A	NCBI36
NG_009164.1:g.93257G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335725.9:c.*1015G>A MANE Select	ENSP00000337353.4:n.*1015G>A
ENST00000335725.8:c.*1015G>A	ENSP00000337353.4:n.*1015G>A
NM_001008744.1:c.*1015G>A	NP_001008744.1:n.*1015G>A
NM_018319.3:c.*1015G>A	NP_060789.2:n.*1015G>A
XM_005267847.2:c.*1015G>A	XP_005267904.1:n.*1015G>A
XM_005267848.1:c.*1015G>A	XP_005267905.1:n.*1015G>A
XM_006720197.2:c.*1015G>A	XP_006720260.1:n.*1015G>A
XM_006720198.2:c.*1015G>A	XP_006720261.1:n.*1015G>A
XM_006720199.1:c.*1015G>A	XP_006720262.1:n.*1015G>A
XM_006720200.2:c.*1015G>A	XP_006720263.1:n.*1015G>A
XM_011536941.1:c.*1015G>A	XP_011535243.1:n.*1015G>A
XM_011536942.1:c.*1015G>A	XP_011535244.1:n.*1015G>A
XM_011536943.1:c.*1015G>A	XP_011535245.1:n.*1015G>A
XM_011536944.1:c.*996G>A	XP_011535246.1:n.*996G>A
NM_001330205.1:c.*996G>A	NP_001317134.1:n.*996G>A
XM_005267848.3:c.*1015G>A	XP_005267905.1:n.*1015G>A
XM_006720197.4:c.*1015G>A	XP_006720260.1:n.*1015G>A
XM_011536942.3:c.*1015G>A	XP_011535244.1:n.*1015G>A
XM_011536944.2:c.*996G>A	XP_011535246.1:n.*996G>A
XM_017021439.2:c.*1015G>A	XP_016876928.1:n.*1015G>A
XM_017021440.2:c.*996G>A	XP_016876929.1:n.*996G>A
XM_024449649.1:c.*1015G>A	XP_024305417.1:n.*1015G>A
XM_024449650.1:c.*1015G>A	XP_024305418.1:n.*1015G>A
XM_024449651.1:c.*1015G>A	XP_024305419.1:n.*1015G>A
XM_024449652.1:c.*1015G>A	XP_024305420.1:n.*1015G>A
XM_024449653.1:c.*1015G>A	XP_024305421.1:n.*1015G>A
XM_024449654.1:c.*1015G>A	XP_024305422.1:n.*1015G>A
XM_024449655.1:c.*1015G>A	XP_024305423.1:n.*1015G>A
XM_024449656.1:c.*1015G>A	XP_024305424.1:n.*1015G>A
XM_024449657.1:c.*1015G>A	XP_024305425.1:n.*1015G>A
XM_024449658.1:c.*1015G>A	XP_024305426.1:n.*1015G>A
XM_024449659.1:c.*996G>A	XP_024305427.1:n.*996G>A
XR_001750427.2:n.3072G>A
XR_943492.3:n.3346G>A
NM_001008744.2:c.*1015G>A	NP_001008744.1:n.*1015G>A
NM_001330205.2:c.*996G>A	NP_001317134.1:n.*996G>A
NM_018319.4:c.*1015G>A MANE Select	NP_060789.2:n.*1015G>A