Canonical Allele Identifier: CA1977888679

Gene: BSCL2 HNRNPUL2-BSCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62692420C= , CM000673.2:g.62692420C=	GRCh38
NC_000011.9:g.62459892C= , CM000673.1:g.62459892C=	GRCh37
NC_000011.8:g.62216468C=	NCBI36
NG_008461.1:g.22155G=
NG_033077.1:g.2480G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000412351.2:n.1011G= (BSCL2)
ENST00000449636.6:c.327G= (BSCL2)	ENSP00000405265.2:p.Leu109=
ENST00000524862.6:c.819G= (BSCL2)	ENSP00000433888.2:p.Leu273=
ENST00000682003.1:n.862G= (BSCL2)
ENST00000682223.1:c.819G= (BSCL2)	ENSP00000508140.1:p.Leu273=
ENST00000682262.1:c.631-999G= (BSCL2)	ENSP00000507103.1:n.631-999G=
ENST00000682555.1:c.737G= (BSCL2)	ENSP00000507814.1:p.Cys246=
ENST00000682644.1:n.1211G= (BSCL2)
ENST00000682794.1:n.1129G= (BSCL2)
ENST00000683025.1:c.*466G= (BSCL2)	ENSP00000507028.1:n.*466G=
ENST00000683296.1:c.819G= (BSCL2)	ENSP00000507725.1:p.Leu273=
ENST00000683368.1:n.1010G= (BSCL2)
ENST00000683494.1:n.1400G= (BSCL2)
ENST00000683846.1:n.1159G= (BSCL2)
ENST00000683892.1:n.1321G= (BSCL2)
ENST00000684067.1:c.819G= (BSCL2)	ENSP00000506799.1:p.Leu273=
ENST00000684115.1:n.1400G= (BSCL2)
ENST00000684258.1:n.1247G= (BSCL2)
ENST00000684285.1:c.*326G= (BSCL2)	ENSP00000507669.1:n.*326G=
ENST00000684475.1:c.684G= (BSCL2)	ENSP00000507429.1:p.Leu228=
ENST00000684609.1:n.1211G= (BSCL2)
ENST00000684720.1:n.1211G= (BSCL2)
ENST00000360796.10:c.819G= (BSCL2) MANE Select	ENSP00000354032.5:p.Leu273=
ENST00000679883.1:c.819G= (BSCL2)	ENSP00000505838.1:p.Leu273=
ENST00000278893.11:c.627G= (BSCL2)	ENSP00000278893.7:p.Leu209=
ENST00000301781.10:c.764G= (BSCL2)	ENSP00000301781.5:p.Cys255=
ENST00000360796.9:c.819G= (BSCL2)	ENSP00000354032.5:p.Leu273=
ENST00000403098.6:c.141G= (BSCL2)	ENSP00000384258.2:p.Leu47=
ENST00000403550.5:c.627G= (BSCL2)	ENSP00000385561.1:p.Leu209=
ENST00000403734.2:c.*870G= (HNRNPUL2-BSCL2)	ENSP00000456010.1:n.*870G=
ENST00000405837.5:c.819G= (BSCL2)	ENSP00000385332.1:p.Leu273=
ENST00000407022.7:c.627G= (BSCL2)	ENSP00000384080.3:p.Leu209=
ENST00000412351.1:n.417G= (BSCL2)
ENST00000421906.5:c.627G= (BSCL2)	ENSP00000413209.1:p.Leu209=
ENST00000448568.6:c.627G= (BSCL2)	ENSP00000413340.2:p.Leu209=
ENST00000468505.5:n.189G= (BSCL2)
ENST00000526426.1:n.343G= (BSCL2)
ENST00000532115.5:n.198G= (BSCL2)
NM_001122955.3:c.819G= (BSCL2)	NP_001116427.1:p.Leu273=
NM_001130702.2:c.627G= (BSCL2)	NP_001124174.2:p.Leu209=
NM_032667.6:c.627G= (BSCL2)	NP_116056.3:p.Leu209=
NR_037946.1:n.3339G= (HNRNPUL2-BSCL2)
NR_037948.1:n.1421G= (BSCL2)
NR_037949.1:n.1421G= (BSCL2)
NM_001122955.4:c.819G= (BSCL2) MANE Select	NP_001116427.1:p.Leu273=
NM_001386027.1:c.819G= (BSCL2)	NP_001372956.1:p.Leu273=
NM_001386028.1:c.819G= (BSCL2)	NP_001372957.1:p.Leu273=