Canonical Allele Identifier: CA883593491
Gene: TSEN34 HGNC NCBI

Linked Data

ClinVar Variation Id: 804160
ClinVar RCV Id: RCV000991058
dbSNP Id: rs1246937494

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.54193291_54193294dup , CM000681.2:g.54193291_54193294dup GRCh38
NC_000019.8:g.59388958_59388961dup NCBI36
NG_015810.2:g.8057_8060dup
NG_033045.2:g.1583_1586dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000396388.3:c.862_865dup MANE Select ENSP00000379671.2:p.Leu289ProfsTer9
ENST00000429671.7:c.862_865dup ENSP00000397402.4:p.Leu289ProfsTer9
ENST00000455798.6:c.862_865dup ENSP00000400743.2:p.Leu289ProfsTer9
ENST00000653273.2:c.841_844dup ENSP00000499319.2:p.Leu282ProfsTer9
ENST00000665674.2:c.841_844dup ENSP00000499684.2:p.Leu282ProfsTer9
ENST00000667261.1:c.862_865dup ENSP00000499595.1:p.Leu289ProfsTer9
ENST00000302937.8:c.862_865dup ENSP00000305524.4:p.Leu289ProfsTer9
ENST00000396383.5:c.862_865dup ENSP00000379667.1:p.Leu289ProfsTer9
ENST00000396388.2:c.862_865dup ENSP00000379671.2:p.Leu289ProfsTer9
ENST00000429671.6:c.871_874dup ENSP00000397402.3:p.Leu292ProfsTer9
ENST00000496583.1:n.1997_2000dup
NM_001077446.3:c.862_865dup NP_001070914.1:p.Leu289ProfsTer9
NM_001282332.1:c.862_865dup NP_001269261.1:p.Leu289ProfsTer9
NM_001282333.1:c.871_874dup NP_001269262.1:p.Leu292ProfsTer9
NM_024075.4:c.862_865dup NP_076980.2:p.Leu289ProfsTer9
XM_005278290.3:c.871_874dup XP_005278347.1:p.Leu292ProfsTer9
XM_011527294.1:c.862_865dup XP_011525596.1:p.Leu289ProfsTer9
XM_011527295.1:c.862_865dup XP_011525597.1:p.Leu289ProfsTer9
XM_005278290.4:c.871_874dup XP_005278347.1:p.Leu292ProfsTer9
XM_011527294.3:c.862_865dup XP_011525596.1:p.Leu289ProfsTer9
NM_001077446.4:c.862_865dup MANE Select NP_001070914.1:p.Leu289ProfsTer9
NM_024075.5:c.862_865dup NP_076980.2:p.Leu289ProfsTer9
NM_001282332.2:c.862_865dup NP_001269261.1:p.Leu289ProfsTer9
NM_001282333.2:c.862_865dup NP_001269262.2:p.Leu289ProfsTer9
NM_001386740.1:c.862_865dup NP_001373669.1:p.Leu289ProfsTer9