Canonical Allele Identifier: CA474868713
Gene: BSCL2 HGNC NCBI
HNRNPUL2-BSCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.62462154A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62694682A>G , CM000673.2:g.62694682A>G GRCh38
NC_000011.9:g.62462154A>G , CM000673.1:g.62462154A>G GRCh37
NC_000011.8:g.62218730A>G NCBI36
NG_008461.1:g.19893T>C
NG_033077.1:g.218T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000412351.2:n.708T>C (BSCL2)
ENST00000449636.6:c.24T>C (BSCL2) ENSP00000405265.2:p.Val8=
ENST00000524862.6:c.516T>C (BSCL2) ENSP00000433888.2:p.Val172=
ENST00000682003.1:n.694T>C (BSCL2)
ENST00000682223.1:c.516T>C (BSCL2) ENSP00000508140.1:p.Val172=
ENST00000682262.1:c.516T>C (BSCL2) ENSP00000507103.1:p.Val172=
ENST00000682555.1:c.516T>C (BSCL2) ENSP00000507814.1:p.Val172=
ENST00000682644.1:n.908T>C (BSCL2)
ENST00000682794.1:n.826T>C (BSCL2)
ENST00000683025.1:c.*163T>C (BSCL2) ENSP00000507028.1:n.*163T>C
ENST00000683296.1:c.516T>C (BSCL2) ENSP00000507725.1:p.Val172=
ENST00000683368.1:n.707T>C (BSCL2)
ENST00000683494.1:n.908T>C (BSCL2)
ENST00000683846.1:n.856T>C (BSCL2)
ENST00000683892.1:n.1018T>C (BSCL2)
ENST00000684067.1:c.516T>C (BSCL2) ENSP00000506799.1:p.Val172=
ENST00000684115.1:n.908T>C (BSCL2)
ENST00000684258.1:n.944T>C (BSCL2)
ENST00000684285.1:c.*23T>C (BSCL2) ENSP00000507669.1:n.*23T>C
ENST00000684475.1:c.516T>C (BSCL2) ENSP00000507429.1:p.Val172=
ENST00000684609.1:n.908T>C (BSCL2)
ENST00000684720.1:n.908T>C (BSCL2)
ENST00000360796.10:c.516T>C (BSCL2) MANE Select ENSP00000354032.5:p.Val172=
ENST00000679883.1:c.516T>C (BSCL2) ENSP00000505838.1:p.Val172=
ENST00000278893.11:c.324T>C (BSCL2) ENSP00000278893.7:p.Val108=
ENST00000301781.10:c.516T>C (BSCL2) ENSP00000301781.5:p.Val172=
ENST00000360796.9:c.516T>C (BSCL2) ENSP00000354032.5:p.Val172=
ENST00000403550.5:c.324T>C (BSCL2) ENSP00000385561.1:p.Val108=
ENST00000403734.2:c.*567T>C (HNRNPUL2-BSCL2) ENSP00000456010.1:n.*567T>C
ENST00000405837.5:c.516T>C (BSCL2) ENSP00000385332.1:p.Val172=
ENST00000407022.7:c.324T>C (BSCL2) ENSP00000384080.3:p.Val108=
ENST00000412351.1:n.114T>C (BSCL2)
ENST00000421906.5:c.324T>C (BSCL2) ENSP00000413209.1:p.Val108=
ENST00000448568.6:c.324T>C (BSCL2) ENSP00000413340.2:p.Val108=
ENST00000524862.5:c.516T>C (BSCL2) ENSP00000433888.1:p.Val172=
ENST00000525000.5:c.148T>C (BSCL2)
ENST00000526426.1:n.31T>C (BSCL2)
ENST00000530900.1:n.316T>C (BSCL2)
ENST00000531524.5:c.117T>C (BSCL2) ENSP00000436026.1:p.Val39=
ENST00000532115.5:n.30T>C (BSCL2)
ENST00000537604.5:n.567T>C (BSCL2)
NM_001122955.3:c.516T>C (BSCL2) NP_001116427.1:p.Val172=
NM_001130702.2:c.324T>C (BSCL2) NP_001124174.2:p.Val108=
NM_032667.6:c.324T>C (BSCL2) NP_116056.3:p.Val108=
NR_037946.1:n.3036T>C (HNRNPUL2-BSCL2)
NR_037948.1:n.1118T>C (BSCL2)
NR_037949.1:n.1118T>C (BSCL2)
NM_001122955.4:c.516T>C (BSCL2) MANE Select NP_001116427.1:p.Val172=
NM_001386027.1:c.516T>C (BSCL2) NP_001372956.1:p.Val172=
NM_001386028.1:c.516T>C (BSCL2) NP_001372957.1:p.Val172=