Canonical Allele Identifier: CA1619508517
Gene: TSBP1 HGNC NCBI
TSBP1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32315086_32315087delinsTG , CM000668.2:g.32315086_32315087delinsTG GRCh38
NC_000006.11:g.32282863_32282864delinsTG , CM000668.1:g.32282863_32282864delinsTG GRCh37
NC_000006.10:g.32390841_32390842delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000533191.6:c.574+685_574+686delinsCA (TSBP1) MANE Select ENSP00000431199.1:n.574+685_574+686delinsCA
ENST00000698834.1:c.441+685_441+686delinsCA (TSBP1)
ENST00000375007.8:c.574+7399_574+7400delinsCA (TSBP1) ENSP00000364146.4:n.574+7399_574+7400delinsCA
ENST00000375015.8:c.577+1307_577+1308delinsCA (TSBP1) ENSP00000364155.4:n.577+1307_577+1308delinsCA
ENST00000442822.6:c.553+685_553+686delinsCA (TSBP1) ENSP00000411164.2:n.553+685_553+686delinsCA
ENST00000447241.6:c.580+7399_580+7400delinsCA (TSBP1) ENSP00000415517.2:n.580+7399_580+7400delinsCA
ENST00000527965.5:c.532+1307_532+1308delinsCA (TSBP1) ENSP00000435103.1:n.532+1307_532+1308delinsCA
ENST00000533191.5:c.574+685_574+686delinsCA (TSBP1) ENSP00000431199.1:n.574+685_574+686delinsCA
ENST00000612031.4:c.580+685_580+686delinsCA (TSBP1) ENSP00000480403.1:n.580+685_580+686delinsCA
ENST00000617061.4:c.571+1307_571+1308delinsCA (TSBP1) ENSP00000482001.1:n.571+1307_571+1308delinsCA
NM_001286474.1:c.574+685_574+686delinsCA (TSBP1) NP_001273403.1:n.574+685_574+686delinsCA
NM_001286475.1:c.532+1307_532+1308delinsCA (TSBP1) NP_001273404.1:n.532+1307_532+1308delinsCA
NM_006781.4:c.580+7399_580+7400delinsCA (TSBP1) NP_006772.3:n.580+7399_580+7400delinsCA
XM_011514235.1:c.578-417_578-416delinsCA (TSBP1) XP_011512537.1:n.578-417_578-416delinsCA
XM_011514236.1:c.578-417_578-416delinsCA (TSBP1) XP_011512538.1:n.578-417_578-416delinsCA
XM_011514237.1:c.613+7399_613+7400delinsCA (TSBP1) XP_011512539.1:n.613+7399_613+7400delinsCA
XM_011514238.1:c.554-417_554-416delinsCA (TSBP1) XP_011512540.1:n.554-417_554-416delinsCA
XM_011514239.1:c.592+7399_592+7400delinsCA (TSBP1) XP_011512541.1:n.592+7399_592+7400delinsCA
XM_011514240.1:c.580+7399_580+7400delinsCA (TSBP1) XP_011512542.1:n.580+7399_580+7400delinsCA
XM_011514241.1:c.577+685_577+686delinsCA (TSBP1) XP_011512543.1:n.577+685_577+686delinsCA
XM_011514242.1:c.574+685_574+686delinsCA (TSBP1) XP_011512544.1:n.574+685_574+686delinsCA
XM_011514243.1:c.556+1307_556+1308delinsCA (TSBP1) XP_011512545.1:n.556+1307_556+1308delinsCA
XM_011514244.1:c.553+685_553+686delinsCA (TSBP1) XP_011512546.1:n.553+685_553+686delinsCA
XM_011514245.1:c.535+7399_535+7400delinsCA (TSBP1) XP_011512547.1:n.535+7399_535+7400delinsCA
XM_011514246.1:c.532+1307_532+1308delinsCA (TSBP1) XP_011512548.1:n.532+1307_532+1308delinsCA
XM_011515039.1:c.422-50694_422-50693delinsTG (TSBP1-AS1) XP_011513341.1:n.422-50694_422-50693delinsTG
XM_011515040.1:c.422-50694_422-50693delinsTG (TSBP1-AS1) XP_011513342.1:n.422-50694_422-50693delinsTG
NR_136244.1:n.441-50694_441-50693delinsTG (TSBP1-AS1)
NR_136245.1:n.243-50694_243-50693delinsTG (TSBP1-AS1)
NR_136246.1:n.243-34426_243-34425delinsTG (TSBP1-AS1)
XM_017010182.1:c.242-417_242-416delinsCA (TSBP1) XP_016865671.1:n.242-417_242-416delinsCA
XM_017010183.1:c.314+685_314+686delinsCA (TSBP1) XP_016865672.1:n.314+685_314+686delinsCA
XM_024446306.1:c.338+685_338+686delinsCA (TSBP1) XP_024302074.1:n.338+685_338+686delinsCA
XM_024446307.1:c.656-417_656-416delinsCA (TSBP1) XP_024302075.1:n.656-417_656-416delinsCA
NM_001286474.2:c.574+685_574+686delinsCA (TSBP1) MANE Select NP_001273403.1:n.574+685_574+686delinsCA
NM_001286475.2:c.532+1307_532+1308delinsCA (TSBP1) NP_001273404.1:n.532+1307_532+1308delinsCA
NM_006781.5:c.580+7399_580+7400delinsCA (TSBP1) NP_006772.3:n.580+7399_580+7400delinsCA