Canonical Allele Identifier: CA823938686

Gene: TSBP1 TSBP1-AS1

Linked Data

• dbSNP Id: rs1379518282
• MyVariant Identifiers: chr6:g.32261211_32261255del (hg19) ; chr6:g.32293434_32293478del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32293452_32293496del , CM000668.2:g.32293452_32293496del	GRCh38
NC_000006.11:g.32261229_32261273del , CM000668.1:g.32261229_32261273del	GRCh37
NC_000006.10:g.32369207_32369251del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000533191.6:c.1189_1233del (TSBP1) MANE Select	ENSP00000431199.1:p.Lys397_Val411del
ENST00000375007.8:c.1189_1233del (TSBP1)	ENSP00000364146.4:p.Lys397_Val411del
ENST00000375015.8:c.1192_1236del (TSBP1)	ENSP00000364155.4:p.Lys398_Val412del
ENST00000442822.6:c.1168_1212del (TSBP1)	ENSP00000411164.2:p.Lys390_Val404del
ENST00000447241.6:c.1195_1239del (TSBP1)	ENSP00000415517.2:p.Lys399_Val413del
ENST00000527965.5:c.1147_1191del (TSBP1)	ENSP00000435103.1:p.Lys383_Val397del
ENST00000533191.5:c.1189_1233del (TSBP1)	ENSP00000431199.1:p.Lys397_Val411del
ENST00000612031.4:c.1195_1239del (TSBP1)	ENSP00000480403.1:p.Lys399_Val413del
ENST00000617061.4:c.1180_1224del (TSBP1)	ENSP00000482001.1:p.Lys394_Val408del
NM_001286474.1:c.1189_1233del (TSBP1)	NP_001273403.1:p.Lys397_Val411del
NM_001286475.1:c.1147_1191del (TSBP1)	NP_001273404.1:p.Lys383_Val397del
NM_006781.4:c.1195_1239del (TSBP1)	NP_006772.3:p.Lys399_Val413del
XM_011514235.1:c.1249_1293del (TSBP1)	XP_011512537.1:p.Lys417_Val431del
XM_011514236.1:c.1249_1293del (TSBP1)	XP_011512538.1:p.Lys417_Val431del
XM_011514237.1:c.1228_1272del (TSBP1)	XP_011512539.1:p.Lys410_Val424del
XM_011514238.1:c.1225_1269del (TSBP1)	XP_011512540.1:p.Lys409_Val423del
XM_011514239.1:c.1207_1251del (TSBP1)	XP_011512541.1:p.Lys403_Val417del
XM_011514240.1:c.1195_1239del (TSBP1)	XP_011512542.1:p.Lys399_Val413del
XM_011514241.1:c.1192_1236del (TSBP1)	XP_011512543.1:p.Lys398_Val412del
XM_011514242.1:c.1189_1233del (TSBP1)	XP_011512544.1:p.Lys397_Val411del
XM_011514243.1:c.1171_1215del (TSBP1)	XP_011512545.1:p.Lys391_Val405del
XM_011514244.1:c.1168_1212del (TSBP1)	XP_011512546.1:p.Lys390_Val404del
XM_011514245.1:c.1150_1194del (TSBP1)	XP_011512547.1:p.Lys384_Val398del
XM_011514246.1:c.1147_1191del (TSBP1)	XP_011512548.1:p.Lys383_Val397del
XM_011515039.1:c.421+30643_421+30687del (TSBP1-AS1)	XP_011513341.1:n.421+30643_421+30687del
XM_011515040.1:c.421+30643_421+30687del (TSBP1-AS1)	XP_011513342.1:n.421+30643_421+30687del
NR_136244.1:n.440+30643_440+30687del (TSBP1-AS1)
NR_136245.1:n.242+38038_242+38082del (TSBP1-AS1)
NR_136246.1:n.242+38038_242+38082del (TSBP1-AS1)
XM_017010182.1:c.913_957del (TSBP1)	XP_016865671.1:p.Lys305_Val319del
XM_024446307.1:c.1327_1371del (TSBP1)	XP_024302075.1:p.Lys443_Val457del
NM_001286474.2:c.1189_1233del (TSBP1) MANE Select	NP_001273403.1:p.Lys397_Val411del
NM_001286475.2:c.1147_1191del (TSBP1)	NP_001273404.1:p.Lys383_Val397del
NM_006781.5:c.1195_1239del (TSBP1)	NP_006772.3:p.Lys399_Val413del