Canonical Allele Identifier: CA380962818
Gene: BSCL2 HGNC NCBI
HNRNPUL2-BSCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62692715T>A , CM000673.2:g.62692715T>A GRCh38
NC_000011.9:g.62460187T>A , CM000673.1:g.62460187T>A GRCh37
NC_000011.8:g.62216763T>A NCBI36
NG_008461.1:g.21860A>T
NG_033077.1:g.2185A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000412351.2:n.905A>T (BSCL2)
ENST00000449636.6:c.221A>T (BSCL2) ENSP00000405265.2:p.Glu74Val
ENST00000524862.6:c.713A>T (BSCL2) ENSP00000433888.2:p.Glu238Val
ENST00000682003.1:n.809-242A>T (BSCL2)
ENST00000682223.1:c.713A>T (BSCL2) ENSP00000508140.1:p.Glu238Val
ENST00000682262.1:c.631-1294A>T (BSCL2) ENSP00000507103.1:n.631-1294A>T
ENST00000682555.1:c.631A>T (BSCL2) ENSP00000507814.1:p.Ser211Cys
ENST00000682644.1:n.1105A>T (BSCL2)
ENST00000682794.1:n.1023A>T (BSCL2)
ENST00000683025.1:c.*360A>T (BSCL2) ENSP00000507028.1:n.*360A>T
ENST00000683296.1:c.713A>T (BSCL2) ENSP00000507725.1:p.Glu238Val
ENST00000683368.1:n.904A>T (BSCL2)
ENST00000683494.1:n.1105A>T (BSCL2)
ENST00000683846.1:n.1053A>T (BSCL2)
ENST00000683892.1:n.1215A>T (BSCL2)
ENST00000684067.1:c.713A>T (BSCL2) ENSP00000506799.1:p.Glu238Val
ENST00000684115.1:n.1105A>T (BSCL2)
ENST00000684258.1:n.1141A>T (BSCL2)
ENST00000684285.1:c.*220A>T (BSCL2) ENSP00000507669.1:n.*220A>T
ENST00000684475.1:c.631-242A>T (BSCL2) ENSP00000507429.1:n.631-242A>T
ENST00000684609.1:n.1105A>T (BSCL2)
ENST00000684720.1:n.1105A>T (BSCL2)
ENST00000360796.10:c.713A>T (BSCL2) MANE Select ENSP00000354032.5:p.Glu238Val
ENST00000679883.1:c.713A>T (BSCL2) ENSP00000505838.1:p.Glu238Val
ENST00000278893.11:c.521A>T (BSCL2) ENSP00000278893.7:p.Glu174Val
ENST00000301781.10:c.658A>T (BSCL2) ENSP00000301781.5:p.Ser220Cys
ENST00000360796.9:c.713A>T (BSCL2) ENSP00000354032.5:p.Glu238Val
ENST00000403098.6:c.35A>T (BSCL2) ENSP00000384258.2:p.Glu12Val
ENST00000403550.5:c.521A>T (BSCL2) ENSP00000385561.1:p.Glu174Val
ENST00000403734.2:c.*764A>T (HNRNPUL2-BSCL2) ENSP00000456010.1:n.*764A>T
ENST00000405837.5:c.713A>T (BSCL2) ENSP00000385332.1:p.Glu238Val
ENST00000407022.7:c.521A>T (BSCL2) ENSP00000384080.3:p.Glu174Val
ENST00000412351.1:n.311A>T (BSCL2)
ENST00000421906.5:c.521A>T (BSCL2) ENSP00000413209.1:p.Glu174Val
ENST00000448568.6:c.521A>T (BSCL2) ENSP00000413340.2:p.Glu174Val
ENST00000468505.5:n.83A>T (BSCL2)
ENST00000526426.1:n.228A>T (BSCL2)
ENST00000531524.5:c.314A>T (BSCL2) ENSP00000436026.1:p.Glu105Val
ENST00000532115.5:n.145-242A>T (BSCL2)
NM_001122955.3:c.713A>T (BSCL2) NP_001116427.1:p.Glu238Val
NM_001130702.2:c.521A>T (BSCL2) NP_001124174.2:p.Glu174Val
NM_032667.6:c.521A>T (BSCL2) NP_116056.3:p.Glu174Val
NR_037946.1:n.3233A>T (HNRNPUL2-BSCL2)
NR_037948.1:n.1315A>T (BSCL2)
NR_037949.1:n.1315A>T (BSCL2)
NM_001122955.4:c.713A>T (BSCL2) MANE Select NP_001116427.1:p.Glu238Val
NM_001386027.1:c.713A>T (BSCL2) NP_001372956.1:p.Glu238Val
NM_001386028.1:c.713A>T (BSCL2) NP_001372957.1:p.Glu238Val