Canonical Allele Identifier: CA474866329

Gene: BSCL2 HNRNPUL2-BSCL2

Linked Data

• MyVariant Identifiers: chr11:g.62460204C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62692732C>A , CM000673.2:g.62692732C>A	GRCh38
NC_000011.9:g.62460204C>A , CM000673.1:g.62460204C>A	GRCh37
NC_000011.8:g.62216780C>A	NCBI36
NG_008461.1:g.21843G>T
NG_033077.1:g.2168G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412351.2:n.888G>T (BSCL2)
ENST00000449636.6:c.204G>T (BSCL2)	ENSP00000405265.2:p.Leu68=
ENST00000524862.6:c.696G>T (BSCL2)	ENSP00000433888.2:p.Leu232=
ENST00000682003.1:n.809-259G>T (BSCL2)
ENST00000682223.1:c.696G>T (BSCL2)	ENSP00000508140.1:p.Leu232=
ENST00000682262.1:c.631-1311G>T (BSCL2)	ENSP00000507103.1:n.631-1311G>T
ENST00000682555.1:c.631-17G>T (BSCL2)	ENSP00000507814.1:n.631-17G>T
ENST00000682644.1:n.1088G>T (BSCL2)
ENST00000682794.1:n.1006G>T (BSCL2)
ENST00000683025.1:c.*343G>T (BSCL2)	ENSP00000507028.1:n.*343G>T
ENST00000683296.1:c.696G>T (BSCL2)	ENSP00000507725.1:p.Leu232=
ENST00000683368.1:n.887G>T (BSCL2)
ENST00000683494.1:n.1088G>T (BSCL2)
ENST00000683846.1:n.1036G>T (BSCL2)
ENST00000683892.1:n.1198G>T (BSCL2)
ENST00000684067.1:c.696G>T (BSCL2)	ENSP00000506799.1:p.Leu232=
ENST00000684115.1:n.1088G>T (BSCL2)
ENST00000684258.1:n.1124G>T (BSCL2)
ENST00000684285.1:c.*203G>T (BSCL2)	ENSP00000507669.1:n.*203G>T
ENST00000684475.1:c.631-259G>T (BSCL2)	ENSP00000507429.1:n.631-259G>T
ENST00000684609.1:n.1088G>T (BSCL2)
ENST00000684720.1:n.1088G>T (BSCL2)
ENST00000360796.10:c.696G>T (BSCL2) MANE Select	ENSP00000354032.5:p.Leu232=
ENST00000679883.1:c.696G>T (BSCL2)	ENSP00000505838.1:p.Leu232=
ENST00000278893.11:c.504G>T (BSCL2)	ENSP00000278893.7:p.Leu168=
ENST00000301781.10:c.641G>T (BSCL2)	ENSP00000301781.5:p.Cys214Phe
ENST00000360796.9:c.696G>T (BSCL2)	ENSP00000354032.5:p.Leu232=
ENST00000403098.6:c.18G>T (BSCL2)	ENSP00000384258.2:p.Leu6=
ENST00000403550.5:c.504G>T (BSCL2)	ENSP00000385561.1:p.Leu168=
ENST00000403734.2:c.*747G>T (HNRNPUL2-BSCL2)	ENSP00000456010.1:n.*747G>T
ENST00000405837.5:c.696G>T (BSCL2)	ENSP00000385332.1:p.Leu232=
ENST00000407022.7:c.504G>T (BSCL2)	ENSP00000384080.3:p.Leu168=
ENST00000412351.1:n.294G>T (BSCL2)
ENST00000421906.5:c.504G>T (BSCL2)	ENSP00000413209.1:p.Leu168=
ENST00000448568.6:c.504G>T (BSCL2)	ENSP00000413340.2:p.Leu168=
ENST00000468505.5:n.66G>T (BSCL2)
ENST00000526426.1:n.211G>T (BSCL2)
ENST00000531524.5:c.297G>T (BSCL2)	ENSP00000436026.1:p.Leu99=
ENST00000532115.5:n.145-259G>T (BSCL2)
NM_001122955.3:c.696G>T (BSCL2)	NP_001116427.1:p.Leu232=
NM_001130702.2:c.504G>T (BSCL2)	NP_001124174.2:p.Leu168=
NM_032667.6:c.504G>T (BSCL2)	NP_116056.3:p.Leu168=
NR_037946.1:n.3216G>T (HNRNPUL2-BSCL2)
NR_037948.1:n.1298G>T (BSCL2)
NR_037949.1:n.1298G>T (BSCL2)
NM_001122955.4:c.696G>T (BSCL2) MANE Select	NP_001116427.1:p.Leu232=
NM_001386027.1:c.696G>T (BSCL2)	NP_001372956.1:p.Leu232=
NM_001386028.1:c.696G>T (BSCL2)	NP_001372957.1:p.Leu232=