Canonical Allele Identifier: CA1977889395

Gene: BSCL2 HNRNPUL2-BSCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62692702C= , CM000673.2:g.62692702C=	GRCh38
NC_000011.9:g.62460174C= , CM000673.1:g.62460174C=	GRCh37
NC_000011.8:g.62216750C=	NCBI36
NG_008461.1:g.21873G=
NG_033077.1:g.2198G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412351.2:n.918G= (BSCL2)
ENST00000449636.6:c.234G= (BSCL2)	ENSP00000405265.2:p.Leu78=
ENST00000524862.6:c.726G= (BSCL2)	ENSP00000433888.2:p.Leu242=
ENST00000682003.1:n.809-229G= (BSCL2)
ENST00000682223.1:c.726G= (BSCL2)	ENSP00000508140.1:p.Leu242=
ENST00000682262.1:c.631-1281G= (BSCL2)	ENSP00000507103.1:n.631-1281G=
ENST00000682555.1:c.644G= (BSCL2)	ENSP00000507814.1:p.Cys215=
ENST00000682644.1:n.1118G= (BSCL2)
ENST00000682794.1:n.1036G= (BSCL2)
ENST00000683025.1:c.*373G= (BSCL2)	ENSP00000507028.1:n.*373G=
ENST00000683296.1:c.726G= (BSCL2)	ENSP00000507725.1:p.Leu242=
ENST00000683368.1:n.917G= (BSCL2)
ENST00000683494.1:n.1118G= (BSCL2)
ENST00000683846.1:n.1066G= (BSCL2)
ENST00000683892.1:n.1228G= (BSCL2)
ENST00000684067.1:c.726G= (BSCL2)	ENSP00000506799.1:p.Leu242=
ENST00000684115.1:n.1118G= (BSCL2)
ENST00000684258.1:n.1154G= (BSCL2)
ENST00000684285.1:c.*233G= (BSCL2)	ENSP00000507669.1:n.*233G=
ENST00000684475.1:c.631-229G= (BSCL2)	ENSP00000507429.1:n.631-229G=
ENST00000684609.1:n.1118G= (BSCL2)
ENST00000684720.1:n.1118G= (BSCL2)
ENST00000360796.10:c.726G= (BSCL2) MANE Select	ENSP00000354032.5:p.Leu242=
ENST00000679883.1:c.726G= (BSCL2)	ENSP00000505838.1:p.Leu242=
ENST00000278893.11:c.534G= (BSCL2)	ENSP00000278893.7:p.Leu178=
ENST00000301781.10:c.671G= (BSCL2)	ENSP00000301781.5:p.Cys224=
ENST00000360796.9:c.726G= (BSCL2)	ENSP00000354032.5:p.Leu242=
ENST00000403098.6:c.48G= (BSCL2)	ENSP00000384258.2:p.Leu16=
ENST00000403550.5:c.534G= (BSCL2)	ENSP00000385561.1:p.Leu178=
ENST00000403734.2:c.*777G= (HNRNPUL2-BSCL2)	ENSP00000456010.1:n.*777G=
ENST00000405837.5:c.726G= (BSCL2)	ENSP00000385332.1:p.Leu242=
ENST00000407022.7:c.534G= (BSCL2)	ENSP00000384080.3:p.Leu178=
ENST00000412351.1:n.324G= (BSCL2)
ENST00000421906.5:c.534G= (BSCL2)	ENSP00000413209.1:p.Leu178=
ENST00000448568.6:c.534G= (BSCL2)	ENSP00000413340.2:p.Leu178=
ENST00000468505.5:n.96G= (BSCL2)
ENST00000526426.1:n.241G= (BSCL2)
ENST00000531524.5:c.327G= (BSCL2)	ENSP00000436026.1:p.Leu109=
ENST00000532115.5:n.145-229G= (BSCL2)
NM_001122955.3:c.726G= (BSCL2)	NP_001116427.1:p.Leu242=
NM_001130702.2:c.534G= (BSCL2)	NP_001124174.2:p.Leu178=
NM_032667.6:c.534G= (BSCL2)	NP_116056.3:p.Leu178=
NR_037946.1:n.3246G= (HNRNPUL2-BSCL2)
NR_037948.1:n.1328G= (BSCL2)
NR_037949.1:n.1328G= (BSCL2)
NM_001122955.4:c.726G= (BSCL2) MANE Select	NP_001116427.1:p.Leu242=
NM_001386027.1:c.726G= (BSCL2)	NP_001372956.1:p.Leu242=
NM_001386028.1:c.726G= (BSCL2)	NP_001372957.1:p.Leu242=