Canonical Allele Identifier: CA1025592687
Gene: SOX10 HGNC NCBI
POLR2F HGNC NCBI

Linked Data

dbSNP Id: rs1932291445

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37978408_37978409del , CM000684.2:g.37978408_37978409del GRCh38
NC_000022.10:g.38374415_38374416del , CM000684.1:g.38374415_38374416del GRCh37
NC_000022.9:g.36704361_36704362del NCBI36
NG_007948.1:g.11124_11125del , LRG_271:g.11124_11125del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698177.1:c.645-274_645-273del (SOX10) ENSP00000513596.1:n.645-274_645-273del
ENST00000690831.1:c.*50+190_*50+191del (SOX10) ENSP00000510381.1:n.*50+190_*50+191del
ENST00000396884.8:c.429-274_429-273del (SOX10) MANE Select ENSP00000380093.2:n.429-274_429-273del
ENST00000360880.6:c.429-274_429-273del (SOX10) ENSP00000354130.2:n.429-274_429-273del
ENST00000396884.6:c.429-274_429-273del (SOX10) ENSP00000380093.2:n.429-274_429-273del
ENST00000405557.5:c.293+11238_293+11239del (POLR2F) ENSP00000384112.1:n.293+11238_293+11239del
ENST00000407936.5:c.294-7746_294-7745del (POLR2F) ENSP00000385725.1:n.294-7746_294-7745del
ENST00000427770.1:c.429-274_429-273del (SOX10) ENSP00000414853.1:n.429-274_429-273del
ENST00000443002.5:c.*38+6098_*38+6099del (POLR2F) ENSP00000406826.1:n.*38+6098_*38+6099del
ENST00000446929.5:c.59-274_59-273del (SOX10)
ENST00000470555.1:n.71-274_71-273del (SOX10)
NM_001301130.1:c.294-7746_294-7745del (POLR2F) NP_001288059.1:n.294-7746_294-7745del
NM_001301131.1:c.293+11238_293+11239del (POLR2F) NP_001288060.1:n.293+11238_293+11239del
NM_006941.3:c.429-274_429-273del , LRG_271t1:c.429-274_429-273del (SOX10) NP_008872.1:n.429-274_429-273del
XR_938243.1:n.158+6098_158+6099del
NM_001363825.1:c.*38+6098_*38+6099del (POLR2F) NP_001350754.1:n.*38+6098_*38+6099del
NM_001301130.2:c.294-7746_294-7745del (POLR2F) NP_001288059.1:n.294-7746_294-7745del
NM_001301131.2:c.293+11238_293+11239del (POLR2F) NP_001288060.1:n.293+11238_293+11239del
NM_006941.4:c.429-274_429-273del (SOX10) MANE Select NP_008872.1:n.429-274_429-273del