Canonical Allele Identifier: CA380961902

Gene: BSCL2 HNRNPUL2-BSCL2

Linked Data

• MyVariant Identifiers: chr11:g.62459848C>G (hg19) ; chr11:g.62692376C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62692376C>G , CM000673.2:g.62692376C>G	GRCh38
NC_000011.9:g.62459848C>G , CM000673.1:g.62459848C>G	GRCh37
NC_000011.8:g.62216424C>G	NCBI36
NG_008461.1:g.22199G>C
NG_033077.1:g.2524G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412351.2:n.1055G>C (BSCL2)
ENST00000449636.6:c.371G>C (BSCL2)	ENSP00000405265.2:p.Arg124Thr
ENST00000524862.6:c.863G>C (BSCL2)	ENSP00000433888.2:p.Arg288Thr
ENST00000682003.1:n.906G>C (BSCL2)
ENST00000682223.1:c.863G>C (BSCL2)	ENSP00000508140.1:p.Arg288Thr
ENST00000682262.1:c.631-955G>C (BSCL2)	ENSP00000507103.1:n.631-955G>C
ENST00000682555.1:c.781G>C (BSCL2)	ENSP00000507814.1:p.Asp261His
ENST00000682644.1:n.1255G>C (BSCL2)
ENST00000682794.1:n.1173G>C (BSCL2)
ENST00000683025.1:c.*510G>C (BSCL2)	ENSP00000507028.1:n.*510G>C
ENST00000683296.1:c.863G>C (BSCL2)	ENSP00000507725.1:p.Arg288Thr
ENST00000683368.1:n.1054G>C (BSCL2)
ENST00000683494.1:n.1444G>C (BSCL2)
ENST00000683846.1:n.1203G>C (BSCL2)
ENST00000683892.1:n.1365G>C (BSCL2)
ENST00000684067.1:c.863G>C (BSCL2)	ENSP00000506799.1:p.Arg288Thr
ENST00000684115.1:n.1444G>C (BSCL2)
ENST00000684258.1:n.1291G>C (BSCL2)
ENST00000684285.1:c.*370G>C (BSCL2)	ENSP00000507669.1:n.*370G>C
ENST00000684475.1:c.728G>C (BSCL2)	ENSP00000507429.1:p.Arg243Thr
ENST00000684609.1:n.1255G>C (BSCL2)
ENST00000684720.1:n.1255G>C (BSCL2)
ENST00000360796.10:c.863G>C (BSCL2) MANE Select	ENSP00000354032.5:p.Arg288Thr
ENST00000679883.1:c.863G>C (BSCL2)	ENSP00000505838.1:p.Arg288Thr
ENST00000278893.11:c.671G>C (BSCL2)	ENSP00000278893.7:p.Arg224Thr
ENST00000301781.10:c.808G>C (BSCL2)	ENSP00000301781.5:p.Asp270His
ENST00000360796.9:c.863G>C (BSCL2)	ENSP00000354032.5:p.Arg288Thr
ENST00000403098.6:c.185G>C (BSCL2)	ENSP00000384258.2:p.Ser62Thr
ENST00000403550.5:c.671G>C (BSCL2)	ENSP00000385561.1:p.Arg224Thr
ENST00000403734.2:c.*914G>C (HNRNPUL2-BSCL2)	ENSP00000456010.1:n.*914G>C
ENST00000405837.5:c.863G>C (BSCL2)	ENSP00000385332.1:p.Arg288Thr
ENST00000407022.7:c.671G>C (BSCL2)	ENSP00000384080.3:p.Arg224Thr
ENST00000412351.1:n.461G>C (BSCL2)
ENST00000421906.5:c.671G>C (BSCL2)	ENSP00000413209.1:p.Arg224Thr
ENST00000448568.6:c.671G>C (BSCL2)
ENST00000468505.5:n.233G>C (BSCL2)
ENST00000532115.5:n.242G>C (BSCL2)
NM_001122955.3:c.863G>C (BSCL2)	NP_001116427.1:p.Arg288Thr
NM_001130702.2:c.671G>C (BSCL2)	NP_001124174.2:p.Arg224Thr
NM_032667.6:c.671G>C (BSCL2)	NP_116056.3:p.Arg224Thr
NR_037946.1:n.3383G>C (HNRNPUL2-BSCL2)
NR_037948.1:n.1465G>C (BSCL2)
NR_037949.1:n.1465G>C (BSCL2)
NM_001122955.4:c.863G>C (BSCL2) MANE Select	NP_001116427.1:p.Arg288Thr
NM_001386027.1:c.863G>C (BSCL2)	NP_001372956.1:p.Arg288Thr
NM_001386028.1:c.863G>C (BSCL2)	NP_001372957.1:p.Arg288Thr