Canonical Allele Identifier: CA380962888

Gene: BSCL2 HNRNPUL2-BSCL2

Linked Data

• MyVariant Identifiers: chr11:g.62460199A>T (hg19) ; chr11:g.62692727A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62692727A>T , CM000673.2:g.62692727A>T	GRCh38
NC_000011.9:g.62460199A>T , CM000673.1:g.62460199A>T	GRCh37
NC_000011.8:g.62216775A>T	NCBI36
NG_008461.1:g.21848T>A
NG_033077.1:g.2173T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412351.2:n.893T>A (BSCL2)
ENST00000449636.6:c.209T>A (BSCL2)	ENSP00000405265.2:p.Phe70Tyr
ENST00000524862.6:c.701T>A (BSCL2)	ENSP00000433888.2:p.Phe234Tyr
ENST00000682003.1:n.809-254T>A (BSCL2)
ENST00000682223.1:c.701T>A (BSCL2)	ENSP00000508140.1:p.Phe234Tyr
ENST00000682262.1:c.631-1306T>A (BSCL2)	ENSP00000507103.1:n.631-1306T>A
ENST00000682555.1:c.631-12T>A (BSCL2)	ENSP00000507814.1:n.631-12T>A
ENST00000682644.1:n.1093T>A (BSCL2)
ENST00000682794.1:n.1011T>A (BSCL2)
ENST00000683025.1:c.*348T>A (BSCL2)	ENSP00000507028.1:n.*348T>A
ENST00000683296.1:c.701T>A (BSCL2)	ENSP00000507725.1:p.Phe234Tyr
ENST00000683368.1:n.892T>A (BSCL2)
ENST00000683494.1:n.1093T>A (BSCL2)
ENST00000683846.1:n.1041T>A (BSCL2)
ENST00000683892.1:n.1203T>A (BSCL2)
ENST00000684067.1:c.701T>A (BSCL2)	ENSP00000506799.1:p.Phe234Tyr
ENST00000684115.1:n.1093T>A (BSCL2)
ENST00000684258.1:n.1129T>A (BSCL2)
ENST00000684285.1:c.*208T>A (BSCL2)	ENSP00000507669.1:n.*208T>A
ENST00000684475.1:c.631-254T>A (BSCL2)	ENSP00000507429.1:n.631-254T>A
ENST00000684609.1:n.1093T>A (BSCL2)
ENST00000684720.1:n.1093T>A (BSCL2)
ENST00000360796.10:c.701T>A (BSCL2) MANE Select	ENSP00000354032.5:p.Phe234Tyr
ENST00000679883.1:c.701T>A (BSCL2)	ENSP00000505838.1:p.Phe234Tyr
ENST00000278893.11:c.509T>A (BSCL2)	ENSP00000278893.7:p.Phe170Tyr
ENST00000301781.10:c.646T>A (BSCL2)	ENSP00000301781.5:p.Leu216Met
ENST00000360796.9:c.701T>A (BSCL2)	ENSP00000354032.5:p.Phe234Tyr
ENST00000403098.6:c.23T>A (BSCL2)	ENSP00000384258.2:p.Phe8Tyr
ENST00000403550.5:c.509T>A (BSCL2)	ENSP00000385561.1:p.Phe170Tyr
ENST00000403734.2:c.*752T>A (HNRNPUL2-BSCL2)	ENSP00000456010.1:n.*752T>A
ENST00000405837.5:c.701T>A (BSCL2)	ENSP00000385332.1:p.Phe234Tyr
ENST00000407022.7:c.509T>A (BSCL2)	ENSP00000384080.3:p.Phe170Tyr
ENST00000412351.1:n.299T>A (BSCL2)
ENST00000421906.5:c.509T>A (BSCL2)	ENSP00000413209.1:p.Phe170Tyr
ENST00000448568.6:c.509T>A (BSCL2)	ENSP00000413340.2:p.Phe170Tyr
ENST00000468505.5:n.71T>A (BSCL2)
ENST00000526426.1:n.216T>A (BSCL2)
ENST00000531524.5:c.302T>A (BSCL2)	ENSP00000436026.1:p.Phe101Tyr
ENST00000532115.5:n.145-254T>A (BSCL2)
NM_001122955.3:c.701T>A (BSCL2)	NP_001116427.1:p.Phe234Tyr
NM_001130702.2:c.509T>A (BSCL2)	NP_001124174.2:p.Phe170Tyr
NM_032667.6:c.509T>A (BSCL2)	NP_116056.3:p.Phe170Tyr
NR_037946.1:n.3221T>A (HNRNPUL2-BSCL2)
NR_037948.1:n.1303T>A (BSCL2)
NR_037949.1:n.1303T>A (BSCL2)
NM_001122955.4:c.701T>A (BSCL2) MANE Select	NP_001116427.1:p.Phe234Tyr
NM_001386027.1:c.701T>A (BSCL2)	NP_001372956.1:p.Phe234Tyr
NM_001386028.1:c.701T>A (BSCL2)	NP_001372957.1:p.Phe234Tyr