Canonical Allele Identifier: CA474864614

Gene: BSCL2 HNRNPUL2-BSCL2

Linked Data

• MyVariant Identifiers: chr11:g.62459853C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62692381C>G , CM000673.2:g.62692381C>G	GRCh38
NC_000011.9:g.62459853C>G , CM000673.1:g.62459853C>G	GRCh37
NC_000011.8:g.62216429C>G	NCBI36
NG_008461.1:g.22194G>C
NG_033077.1:g.2519G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000412351.2:n.1050G>C (BSCL2)
ENST00000449636.6:c.366G>C (BSCL2)	ENSP00000405265.2:p.Gly122=
ENST00000524862.6:c.858G>C (BSCL2)	ENSP00000433888.2:p.Gly286=
ENST00000682003.1:n.901G>C (BSCL2)
ENST00000682223.1:c.858G>C (BSCL2)	ENSP00000508140.1:p.Gly286=
ENST00000682262.1:c.631-960G>C (BSCL2)	ENSP00000507103.1:n.631-960G>C
ENST00000682555.1:c.776G>C (BSCL2)	ENSP00000507814.1:p.Gly259Ala
ENST00000682644.1:n.1250G>C (BSCL2)
ENST00000682794.1:n.1168G>C (BSCL2)
ENST00000683025.1:c.*505G>C (BSCL2)	ENSP00000507028.1:n.*505G>C
ENST00000683296.1:c.858G>C (BSCL2)	ENSP00000507725.1:p.Gly286=
ENST00000683368.1:n.1049G>C (BSCL2)
ENST00000683494.1:n.1439G>C (BSCL2)
ENST00000683846.1:n.1198G>C (BSCL2)
ENST00000683892.1:n.1360G>C (BSCL2)
ENST00000684067.1:c.858G>C (BSCL2)	ENSP00000506799.1:p.Gly286=
ENST00000684115.1:n.1439G>C (BSCL2)
ENST00000684258.1:n.1286G>C (BSCL2)
ENST00000684285.1:c.*365G>C (BSCL2)	ENSP00000507669.1:n.*365G>C
ENST00000684475.1:c.723G>C (BSCL2)	ENSP00000507429.1:p.Gly241=
ENST00000684609.1:n.1250G>C (BSCL2)
ENST00000684720.1:n.1250G>C (BSCL2)
ENST00000360796.10:c.858G>C (BSCL2) MANE Select	ENSP00000354032.5:p.Gly286=
ENST00000679883.1:c.858G>C (BSCL2)	ENSP00000505838.1:p.Gly286=
ENST00000278893.11:c.666G>C (BSCL2)	ENSP00000278893.7:p.Gly222=
ENST00000301781.10:c.803G>C (BSCL2)	ENSP00000301781.5:p.Gly268Ala
ENST00000360796.9:c.858G>C (BSCL2)	ENSP00000354032.5:p.Gly286=
ENST00000403098.6:c.180G>C (BSCL2)	ENSP00000384258.2:p.Gly60=
ENST00000403550.5:c.666G>C (BSCL2)	ENSP00000385561.1:p.Gly222=
ENST00000403734.2:c.*909G>C (HNRNPUL2-BSCL2)	ENSP00000456010.1:n.*909G>C
ENST00000405837.5:c.858G>C (BSCL2)	ENSP00000385332.1:p.Gly286=
ENST00000407022.7:c.666G>C (BSCL2)	ENSP00000384080.3:p.Gly222=
ENST00000412351.1:n.456G>C (BSCL2)
ENST00000421906.5:c.666G>C (BSCL2)	ENSP00000413209.1:p.Gly222=
ENST00000448568.6:c.666G>C (BSCL2)	ENSP00000413340.2:p.Gly222=
ENST00000468505.5:n.228G>C (BSCL2)
ENST00000532115.5:n.237G>C (BSCL2)
NM_001122955.3:c.858G>C (BSCL2)	NP_001116427.1:p.Gly286=
NM_001130702.2:c.666G>C (BSCL2)	NP_001124174.2:p.Gly222=
NM_032667.6:c.666G>C (BSCL2)	NP_116056.3:p.Gly222=
NR_037946.1:n.3378G>C (HNRNPUL2-BSCL2)
NR_037948.1:n.1460G>C (BSCL2)
NR_037949.1:n.1460G>C (BSCL2)
NM_001122955.4:c.858G>C (BSCL2) MANE Select	NP_001116427.1:p.Gly286=
NM_001386027.1:c.858G>C (BSCL2)	NP_001372956.1:p.Gly286=
NM_001386028.1:c.858G>C (BSCL2)	NP_001372957.1:p.Gly286=