Canonical Allele Identifier: CA136936549

Gene: TSBP1 TSBP1-AS1

Linked Data

• dbSNP Id: rs749627685
• MyVariant Identifiers: chr6:g.32282934_32282935insTGAAA (hg19) ; chr6:g.32315157_32315158insTGAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32315158_32315162dup , CM000668.2:g.32315158_32315162dup	GRCh38
NC_000006.11:g.32282935_32282939dup , CM000668.1:g.32282935_32282939dup	GRCh37
NC_000006.10:g.32390913_32390917dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000533191.6:c.574+610_574+614dup (TSBP1) MANE Select	ENSP00000431199.1:n.574+610_574+614dup
ENST00000698834.1:c.441+610_441+614dup (TSBP1)
ENST00000375007.8:c.574+7324_574+7328dup (TSBP1)	ENSP00000364146.4:n.574+7324_574+7328dup
ENST00000375015.8:c.577+1232_577+1236dup (TSBP1)	ENSP00000364155.4:n.577+1232_577+1236dup
ENST00000442822.6:c.553+610_553+614dup (TSBP1)	ENSP00000411164.2:n.553+610_553+614dup
ENST00000447241.6:c.580+7324_580+7328dup (TSBP1)	ENSP00000415517.2:n.580+7324_580+7328dup
ENST00000527965.5:c.532+1232_532+1236dup (TSBP1)	ENSP00000435103.1:n.532+1232_532+1236dup
ENST00000533191.5:c.574+610_574+614dup (TSBP1)	ENSP00000431199.1:n.574+610_574+614dup
ENST00000612031.4:c.580+610_580+614dup (TSBP1)	ENSP00000480403.1:n.580+610_580+614dup
ENST00000617061.4:c.571+1232_571+1236dup (TSBP1)	ENSP00000482001.1:n.571+1232_571+1236dup
NM_001286474.1:c.574+610_574+614dup (TSBP1)	NP_001273403.1:n.574+610_574+614dup
NM_001286475.1:c.532+1232_532+1236dup (TSBP1)	NP_001273404.1:n.532+1232_532+1236dup
NM_006781.4:c.580+7324_580+7328dup (TSBP1)	NP_006772.3:n.580+7324_580+7328dup
XM_011514235.1:c.578-492_578-488dup (TSBP1)	XP_011512537.1:n.578-492_578-488dup
XM_011514236.1:c.578-492_578-488dup (TSBP1)	XP_011512538.1:n.578-492_578-488dup
XM_011514237.1:c.613+7324_613+7328dup (TSBP1)	XP_011512539.1:n.613+7324_613+7328dup
XM_011514238.1:c.554-492_554-488dup (TSBP1)	XP_011512540.1:n.554-492_554-488dup
XM_011514239.1:c.592+7324_592+7328dup (TSBP1)	XP_011512541.1:n.592+7324_592+7328dup
XM_011514240.1:c.580+7324_580+7328dup (TSBP1)	XP_011512542.1:n.580+7324_580+7328dup
XM_011514241.1:c.577+610_577+614dup (TSBP1)	XP_011512543.1:n.577+610_577+614dup
XM_011514242.1:c.574+610_574+614dup (TSBP1)	XP_011512544.1:n.574+610_574+614dup
XM_011514243.1:c.556+1232_556+1236dup (TSBP1)	XP_011512545.1:n.556+1232_556+1236dup
XM_011514244.1:c.553+610_553+614dup (TSBP1)	XP_011512546.1:n.553+610_553+614dup
XM_011514245.1:c.535+7324_535+7328dup (TSBP1)	XP_011512547.1:n.535+7324_535+7328dup
XM_011514246.1:c.532+1232_532+1236dup (TSBP1)	XP_011512548.1:n.532+1232_532+1236dup
XM_011515039.1:c.422-50622_422-50618dup (TSBP1-AS1)	XP_011513341.1:n.422-50622_422-50618dup
XM_011515040.1:c.422-50622_422-50618dup (TSBP1-AS1)	XP_011513342.1:n.422-50622_422-50618dup
NR_136244.1:n.441-50622_441-50618dup (TSBP1-AS1)
NR_136245.1:n.243-50622_243-50618dup (TSBP1-AS1)
NR_136246.1:n.243-34354_243-34350dup (TSBP1-AS1)
XM_017010182.1:c.242-492_242-488dup (TSBP1)	XP_016865671.1:n.242-492_242-488dup
XM_017010183.1:c.314+610_314+614dup (TSBP1)	XP_016865672.1:n.314+610_314+614dup
XM_024446306.1:c.338+610_338+614dup (TSBP1)	XP_024302074.1:n.338+610_338+614dup
XM_024446307.1:c.656-492_656-488dup (TSBP1)	XP_024302075.1:n.656-492_656-488dup
NM_001286474.2:c.574+610_574+614dup (TSBP1) MANE Select	NP_001273403.1:n.574+610_574+614dup
NM_001286475.2:c.532+1232_532+1236dup (TSBP1)	NP_001273404.1:n.532+1232_532+1236dup
NM_006781.5:c.580+7324_580+7328dup (TSBP1)	NP_006772.3:n.580+7324_580+7328dup