Canonical Allele Identifier: CA29580421

Gene: SELENBP1

Linked Data

• dbSNP Id: rs140824562
• MyVariant Identifiers: chr1:g.151344460_151344461insGGCATTCTGCCAGCTC (hg19) ; chr1:g.151371984_151371985insGGCATTCTGCCAGCTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151371985_151371986insGCATTCTGCCAGCTCG , CM000663.2:g.151371985_151371986insGCATTCTGCCAGCTCG	GRCh38
NC_000001.10:g.151344461_151344462insGCATTCTGCCAGCTCG , CM000663.1:g.151344461_151344462insGCATTCTGCCAGCTCG	GRCh37
NC_000001.9:g.149611085_149611086insGCATTCTGCCAGCTCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368868.10:c.4+653_4+654insGAGCTGGCAGAATGCC MANE Select	ENSP00000357861.5:n.4+653_4+654insGAGCTGGCAGAATGCC
ENST00000368868.9:c.4+653_4+654insGAGCTGGCAGAATGCC	ENSP00000357861.5:n.4+653_4+654insGAGCTGGCAGAATGCC
ENST00000423070.5:c.-80+653_-80+654insGAGCTGGCAGAATGCC	ENSP00000416206.1:n.-80+653_-80+654insGAGCTGGCAGAATGCC
ENST00000426705.6:c.-80+653_-80+654insGAGCTGGCAGAATGCC	ENSP00000397261.2:n.-80+653_-80+654insGAGCTGGCAGAATGCC
ENST00000427977.6:c.4+653_4+654insGAGCTGGCAGAATGCC	ENSP00000412816.1:n.4+653_4+654insGAGCTGGCAGAATGCC
ENST00000443708.5:c.4+653_4+654insGAGCTGGCAGAATGCC	ENSP00000402531.1:n.4+653_4+654insGAGCTGGCAGAATGCC
ENST00000447402.7:c.4+653_4+654insGAGCTGGCAGAATGCC	ENSP00000413960.3:n.4+653_4+654insGAGCTGGCAGAATGCC
ENST00000455397.5:c.4+653_4+654insGAGCTGGCAGAATGCC	ENSP00000395637.1:n.4+653_4+654insGAGCTGGCAGAATGCC
ENST00000455839.5:c.4+653_4+654insGAGCTGGCAGAATGCC	ENSP00000390433.1:n.4+653_4+654insGAGCTGGCAGAATGCC
ENST00000458566.5:c.4+653_4+654insGAGCTGGCAGAATGCC	ENSP00000406222.1:n.4+653_4+654insGAGCTGGCAGAATGCC
ENST00000463664.5:n.57+653_57+654insGAGCTGGCAGAATGCC
ENST00000470345.5:n.69+653_69+654insGAGCTGGCAGAATGCC
ENST00000473693.5:n.68+653_68+654insGAGCTGGCAGAATGCC
ENST00000474352.5:n.68+653_68+654insGAGCTGGCAGAATGCC
ENST00000492643.5:n.70+653_70+654insGAGCTGGCAGAATGCC
ENST00000493560.5:n.57+653_57+654insGAGCTGGCAGAATGCC
ENST00000498494.1:n.54+653_54+654insGAGCTGGCAGAATGCC
NM_001258288.1:c.4+653_4+654insGAGCTGGCAGAATGCC	NP_001245217.1:n.4+653_4+654insGAGCTGGCAGAATGCC
NM_001258289.1:c.-80+653_-80+654insGAGCTGGCAGAATGCC	NP_001245218.1:n.-80+653_-80+654insGAGCTGGCAGAATGCC
NM_003944.3:c.4+653_4+654insGAGCTGGCAGAATGCC	NP_003935.2:n.4+653_4+654insGAGCTGGCAGAATGCC
XM_011510110.1:c.-35+653_-35+654insGAGCTGGCAGAATGCC	XP_011508412.1:n.-35+653_-35+654insGAGCTGGCAGAATGCC
XR_921993.1:n.84+653_84+654insGAGCTGGCAGAATGCC
XM_024450671.1:c.-1161+653_-1161+654insGAGCTGGCAGAATGCC	XP_024306439.1:n.-1161+653_-1161+654insGAGCTGGCAGAATGCC
XR_002957987.1:n.88+653_88+654insGAGCTGGCAGAATGCC
XR_921993.2:n.76+653_76+654insGAGCTGGCAGAATGCC
NM_003944.4:c.4+653_4+654insGAGCTGGCAGAATGCC MANE Select	NP_003935.2:n.4+653_4+654insGAGCTGGCAGAATGCC
NM_001258288.2:c.4+653_4+654insGAGCTGGCAGAATGCC	NP_001245217.1:n.4+653_4+654insGAGCTGGCAGAATGCC
NM_001258289.2:c.-80+653_-80+654insGAGCTGGCAGAATGCC	NP_001245218.1:n.-80+653_-80+654insGAGCTGGCAGAATGCC