Canonical Allele Identifier: CA380962723

Gene: BSCL2 HNRNPUL2-BSCL2

Linked Data

• MyVariant Identifiers: chr11:g.62460173G>C (hg19) ; chr11:g.62692701G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62692701G>C , CM000673.2:g.62692701G>C	GRCh38
NC_000011.9:g.62460173G>C , CM000673.1:g.62460173G>C	GRCh37
NC_000011.8:g.62216749G>C	NCBI36
NG_008461.1:g.21874C>G
NG_033077.1:g.2199C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412351.2:n.919C>G (BSCL2)
ENST00000449636.6:c.235C>G (BSCL2)	ENSP00000405265.2:p.Leu79Val
ENST00000524862.6:c.727C>G (BSCL2)	ENSP00000433888.2:p.Leu243Val
ENST00000682003.1:n.809-228C>G (BSCL2)
ENST00000682223.1:c.727C>G (BSCL2)	ENSP00000508140.1:p.Leu243Val
ENST00000682262.1:c.631-1280C>G (BSCL2)	ENSP00000507103.1:n.631-1280C>G
ENST00000682555.1:c.645C>G (BSCL2)	ENSP00000507814.1:p.Cys215Trp
ENST00000682644.1:n.1119C>G (BSCL2)
ENST00000682794.1:n.1037C>G (BSCL2)
ENST00000683025.1:c.*374C>G (BSCL2)	ENSP00000507028.1:n.*374C>G
ENST00000683296.1:c.727C>G (BSCL2)	ENSP00000507725.1:p.Leu243Val
ENST00000683368.1:n.918C>G (BSCL2)
ENST00000683494.1:n.1119C>G (BSCL2)
ENST00000683846.1:n.1067C>G (BSCL2)
ENST00000683892.1:n.1229C>G (BSCL2)
ENST00000684067.1:c.727C>G (BSCL2)	ENSP00000506799.1:p.Leu243Val
ENST00000684115.1:n.1119C>G (BSCL2)
ENST00000684258.1:n.1155C>G (BSCL2)
ENST00000684285.1:c.*234C>G (BSCL2)	ENSP00000507669.1:n.*234C>G
ENST00000684475.1:c.631-228C>G (BSCL2)	ENSP00000507429.1:n.631-228C>G
ENST00000684609.1:n.1119C>G (BSCL2)
ENST00000684720.1:n.1119C>G (BSCL2)
ENST00000360796.10:c.727C>G (BSCL2) MANE Select	ENSP00000354032.5:p.Leu243Val
ENST00000679883.1:c.727C>G (BSCL2)	ENSP00000505838.1:p.Leu243Val
ENST00000278893.11:c.535C>G (BSCL2)	ENSP00000278893.7:p.Leu179Val
ENST00000301781.10:c.672C>G (BSCL2)	ENSP00000301781.5:p.Cys224Trp
ENST00000360796.9:c.727C>G (BSCL2)	ENSP00000354032.5:p.Leu243Val
ENST00000403098.6:c.49C>G (BSCL2)	ENSP00000384258.2:p.Leu17Val
ENST00000403550.5:c.535C>G (BSCL2)	ENSP00000385561.1:p.Leu179Val
ENST00000403734.2:c.*778C>G (HNRNPUL2-BSCL2)	ENSP00000456010.1:n.*778C>G
ENST00000405837.5:c.727C>G (BSCL2)	ENSP00000385332.1:p.Leu243Val
ENST00000407022.7:c.535C>G (BSCL2)	ENSP00000384080.3:p.Leu179Val
ENST00000412351.1:n.325C>G (BSCL2)
ENST00000421906.5:c.535C>G (BSCL2)	ENSP00000413209.1:p.Leu179Val
ENST00000448568.6:c.535C>G (BSCL2)	ENSP00000413340.2:p.Leu179Val
ENST00000468505.5:n.97C>G (BSCL2)
ENST00000526426.1:n.242C>G (BSCL2)
ENST00000531524.5:c.328C>G (BSCL2)	ENSP00000436026.1:p.Leu110Val
ENST00000532115.5:n.145-228C>G (BSCL2)
NM_001122955.3:c.727C>G (BSCL2)	NP_001116427.1:p.Leu243Val
NM_001130702.2:c.535C>G (BSCL2)	NP_001124174.2:p.Leu179Val
NM_032667.6:c.535C>G (BSCL2)	NP_116056.3:p.Leu179Val
NR_037946.1:n.3247C>G (HNRNPUL2-BSCL2)
NR_037948.1:n.1329C>G (BSCL2)
NR_037949.1:n.1329C>G (BSCL2)
NM_001122955.4:c.727C>G (BSCL2) MANE Select	NP_001116427.1:p.Leu243Val
NM_001386027.1:c.727C>G (BSCL2)	NP_001372956.1:p.Leu243Val
NM_001386028.1:c.727C>G (BSCL2)	NP_001372957.1:p.Leu243Val