Canonical Allele Identifier: CA411500124
Gene: SOX10 HGNC NCBI
POLR2F HGNC NCBI

Linked Data

ClinVar Variation Id: 488043
ClinVar RCV Id: RCV000626402
dbSNP Id: rs1555939415

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37983382T>G , CM000684.2:g.37983382T>G GRCh38
NC_000022.10:g.38379389T>G , CM000684.1:g.38379389T>G GRCh37
NC_000022.9:g.36709335T>G NCBI36
NG_007948.1:g.6151A>C , LRG_271:g.6151A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698177.1:c.619A>C (SOX10) ENSP00000513596.1:p.Ser207Arg
ENST00000690831.1:c.403A>C (SOX10) ENSP00000510381.1:p.Ser135Arg
ENST00000396884.8:c.403A>C (SOX10) MANE Select ENSP00000380093.2:p.Ser135Arg
ENST00000652356.1:n.692A>C (SOX10)
ENST00000360880.6:c.403A>C (SOX10) ENSP00000354130.2:p.Ser135Arg
ENST00000396884.6:c.403A>C (SOX10) ENSP00000380093.2:p.Ser135Arg
ENST00000405557.5:c.293+16212T>G (POLR2F) ENSP00000384112.1:n.293+16212T>G
ENST00000407936.5:c.294-2772T>G (POLR2F) ENSP00000385725.1:n.294-2772T>G
ENST00000427770.1:c.403A>C (SOX10) ENSP00000414853.1:p.Ser135Arg
ENST00000443002.5:c.*39-1670T>G (POLR2F) ENSP00000406826.1:n.*39-1670T>G
ENST00000446929.5:c.33A>C (SOX10)
ENST00000470555.1:n.70+957A>C (SOX10)
NM_001301130.1:c.294-2772T>G (POLR2F) NP_001288059.1:n.294-2772T>G
NM_001301131.1:c.293+16212T>G (POLR2F) NP_001288060.1:n.293+16212T>G
NM_006941.3:c.403A>C , LRG_271t1:c.403A>C (SOX10) NP_008872.1:p.Ser135Arg
XR_938243.1:n.158+11072T>G
NM_001363825.1:c.*38+11072T>G (POLR2F) NP_001350754.1:n.*38+11072T>G
NM_001301130.2:c.294-2772T>G (POLR2F) NP_001288059.1:n.294-2772T>G
NM_001301131.2:c.293+16212T>G (POLR2F) NP_001288060.1:n.293+16212T>G
NM_006941.4:c.403A>C (SOX10) MANE Select NP_008872.1:p.Ser135Arg