Canonical Allele Identifier: CA380962138
Gene: BSCL2 HGNC NCBI
HNRNPUL2-BSCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62692428T>C , CM000673.2:g.62692428T>C GRCh38
NC_000011.9:g.62459900T>C , CM000673.1:g.62459900T>C GRCh37
NC_000011.8:g.62216476T>C NCBI36
NG_008461.1:g.22147A>G
NG_033077.1:g.2472A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000412351.2:n.1003A>G (BSCL2)
ENST00000449636.6:c.319A>G (BSCL2) ENSP00000405265.2:p.Ile107Val
ENST00000524862.6:c.811A>G (BSCL2) ENSP00000433888.2:p.Ile271Val
ENST00000682003.1:n.854A>G (BSCL2)
ENST00000682223.1:c.811A>G (BSCL2) ENSP00000508140.1:p.Ile271Val
ENST00000682262.1:c.631-1007A>G (BSCL2) ENSP00000507103.1:n.631-1007A>G
ENST00000682555.1:c.729A>G (BSCL2) ENSP00000507814.1:p.Ala243=
ENST00000682644.1:n.1203A>G (BSCL2)
ENST00000682794.1:n.1121A>G (BSCL2)
ENST00000683025.1:c.*458A>G (BSCL2) ENSP00000507028.1:n.*458A>G
ENST00000683296.1:c.811A>G (BSCL2) ENSP00000507725.1:p.Ile271Val
ENST00000683368.1:n.1002A>G (BSCL2)
ENST00000683494.1:n.1392A>G (BSCL2)
ENST00000683846.1:n.1151A>G (BSCL2)
ENST00000683892.1:n.1313A>G (BSCL2)
ENST00000684067.1:c.811A>G (BSCL2) ENSP00000506799.1:p.Ile271Val
ENST00000684115.1:n.1392A>G (BSCL2)
ENST00000684258.1:n.1239A>G (BSCL2)
ENST00000684285.1:c.*318A>G (BSCL2) ENSP00000507669.1:n.*318A>G
ENST00000684475.1:c.676A>G (BSCL2) ENSP00000507429.1:p.Ile226Val
ENST00000684609.1:n.1203A>G (BSCL2)
ENST00000684720.1:n.1203A>G (BSCL2)
ENST00000360796.10:c.811A>G (BSCL2) MANE Select ENSP00000354032.5:p.Ile271Val
ENST00000679883.1:c.811A>G (BSCL2) ENSP00000505838.1:p.Ile271Val
ENST00000278893.11:c.619A>G (BSCL2) ENSP00000278893.7:p.Ile207Val
ENST00000301781.10:c.756A>G (BSCL2) ENSP00000301781.5:p.Ala252=
ENST00000360796.9:c.811A>G (BSCL2) ENSP00000354032.5:p.Ile271Val
ENST00000403098.6:c.133A>G (BSCL2) ENSP00000384258.2:p.Ile45Val
ENST00000403550.5:c.619A>G (BSCL2) ENSP00000385561.1:p.Ile207Val
ENST00000403734.2:c.*862A>G (HNRNPUL2-BSCL2) ENSP00000456010.1:n.*862A>G
ENST00000405837.5:c.811A>G (BSCL2) ENSP00000385332.1:p.Ile271Val
ENST00000407022.7:c.619A>G (BSCL2) ENSP00000384080.3:p.Ile207Val
ENST00000412351.1:n.409A>G (BSCL2)
ENST00000421906.5:c.619A>G (BSCL2) ENSP00000413209.1:p.Ile207Val
ENST00000448568.6:c.619A>G (BSCL2) ENSP00000413340.2:p.Ile207Val
ENST00000468505.5:n.181A>G (BSCL2)
ENST00000526426.1:n.335A>G (BSCL2)
ENST00000532115.5:n.190A>G (BSCL2)
NM_001122955.3:c.811A>G (BSCL2) NP_001116427.1:p.Ile271Val
NM_001130702.2:c.619A>G (BSCL2) NP_001124174.2:p.Ile207Val
NM_032667.6:c.619A>G (BSCL2) NP_116056.3:p.Ile207Val
NR_037946.1:n.3331A>G (HNRNPUL2-BSCL2)
NR_037948.1:n.1413A>G (BSCL2)
NR_037949.1:n.1413A>G (BSCL2)
NM_001122955.4:c.811A>G (BSCL2) MANE Select NP_001116427.1:p.Ile271Val
NM_001386027.1:c.811A>G (BSCL2) NP_001372956.1:p.Ile271Val
NM_001386028.1:c.811A>G (BSCL2) NP_001372957.1:p.Ile271Val