Canonical Allele Identifier: CA1619508554
Gene: TSBP1 HGNC NCBI
TSBP1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32315201_32315202delinsCA , CM000668.2:g.32315201_32315202delinsCA GRCh38
NC_000006.11:g.32282978_32282979delinsCA , CM000668.1:g.32282978_32282979delinsCA GRCh37
NC_000006.10:g.32390956_32390957delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000533191.6:c.574+570_574+571delinsTG (TSBP1) MANE Select ENSP00000431199.1:n.574+570_574+571delinsTG
ENST00000698834.1:c.441+570_441+571delinsTG (TSBP1)
ENST00000375007.8:c.574+7284_574+7285delinsTG (TSBP1) ENSP00000364146.4:n.574+7284_574+7285delinsTG
ENST00000375015.8:c.577+1192_577+1193delinsTG (TSBP1) ENSP00000364155.4:n.577+1192_577+1193delinsTG
ENST00000442822.6:c.553+570_553+571delinsTG (TSBP1) ENSP00000411164.2:n.553+570_553+571delinsTG
ENST00000447241.6:c.580+7284_580+7285delinsTG (TSBP1) ENSP00000415517.2:n.580+7284_580+7285delinsTG
ENST00000527965.5:c.532+1192_532+1193delinsTG (TSBP1) ENSP00000435103.1:n.532+1192_532+1193delinsTG
ENST00000533191.5:c.574+570_574+571delinsTG (TSBP1) ENSP00000431199.1:n.574+570_574+571delinsTG
ENST00000612031.4:c.580+570_580+571delinsTG (TSBP1) ENSP00000480403.1:n.580+570_580+571delinsTG
ENST00000617061.4:c.571+1192_571+1193delinsTG (TSBP1) ENSP00000482001.1:n.571+1192_571+1193delinsTG
NM_001286474.1:c.574+570_574+571delinsTG (TSBP1) NP_001273403.1:n.574+570_574+571delinsTG
NM_001286475.1:c.532+1192_532+1193delinsTG (TSBP1) NP_001273404.1:n.532+1192_532+1193delinsTG
NM_006781.4:c.580+7284_580+7285delinsTG (TSBP1) NP_006772.3:n.580+7284_580+7285delinsTG
XM_011514235.1:c.578-532_578-531delinsTG (TSBP1) XP_011512537.1:n.578-532_578-531delinsTG
XM_011514236.1:c.578-532_578-531delinsTG (TSBP1) XP_011512538.1:n.578-532_578-531delinsTG
XM_011514237.1:c.613+7284_613+7285delinsTG (TSBP1) XP_011512539.1:n.613+7284_613+7285delinsTG
XM_011514238.1:c.554-532_554-531delinsTG (TSBP1) XP_011512540.1:n.554-532_554-531delinsTG
XM_011514239.1:c.592+7284_592+7285delinsTG (TSBP1) XP_011512541.1:n.592+7284_592+7285delinsTG
XM_011514240.1:c.580+7284_580+7285delinsTG (TSBP1) XP_011512542.1:n.580+7284_580+7285delinsTG
XM_011514241.1:c.577+570_577+571delinsTG (TSBP1) XP_011512543.1:n.577+570_577+571delinsTG
XM_011514242.1:c.574+570_574+571delinsTG (TSBP1) XP_011512544.1:n.574+570_574+571delinsTG
XM_011514243.1:c.556+1192_556+1193delinsTG (TSBP1) XP_011512545.1:n.556+1192_556+1193delinsTG
XM_011514244.1:c.553+570_553+571delinsTG (TSBP1) XP_011512546.1:n.553+570_553+571delinsTG
XM_011514245.1:c.535+7284_535+7285delinsTG (TSBP1) XP_011512547.1:n.535+7284_535+7285delinsTG
XM_011514246.1:c.532+1192_532+1193delinsTG (TSBP1) XP_011512548.1:n.532+1192_532+1193delinsTG
XM_011515039.1:c.422-50579_422-50578delinsCA (TSBP1-AS1) XP_011513341.1:n.422-50579_422-50578delinsCA
XM_011515040.1:c.422-50579_422-50578delinsCA (TSBP1-AS1) XP_011513342.1:n.422-50579_422-50578delinsCA
NR_136244.1:n.441-50579_441-50578delinsCA (TSBP1-AS1)
NR_136245.1:n.243-50579_243-50578delinsCA (TSBP1-AS1)
NR_136246.1:n.243-34311_243-34310delinsCA (TSBP1-AS1)
XM_017010182.1:c.242-532_242-531delinsTG (TSBP1) XP_016865671.1:n.242-532_242-531delinsTG
XM_017010183.1:c.314+570_314+571delinsTG (TSBP1) XP_016865672.1:n.314+570_314+571delinsTG
XM_024446306.1:c.338+570_338+571delinsTG (TSBP1) XP_024302074.1:n.338+570_338+571delinsTG
XM_024446307.1:c.656-532_656-531delinsTG (TSBP1) XP_024302075.1:n.656-532_656-531delinsTG
NM_001286474.2:c.574+570_574+571delinsTG (TSBP1) MANE Select NP_001273403.1:n.574+570_574+571delinsTG
NM_001286475.2:c.532+1192_532+1193delinsTG (TSBP1) NP_001273404.1:n.532+1192_532+1193delinsTG
NM_006781.5:c.580+7284_580+7285delinsTG (TSBP1) NP_006772.3:n.580+7284_580+7285delinsTG