Canonical Allele Identifier: CA2656621185
Gene: SOX10 HGNC NCBI
POLR2F HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37973376A>T , CM000684.2:g.37973376A>T GRCh38
NC_000022.10:g.38369383A>T , CM000684.1:g.38369383A>T GRCh37
NC_000022.9:g.36699329A>T NCBI36
NG_007948.1:g.16157T>A , LRG_271:g.16157T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698177.1:c.*119T>A (SOX10) ENSP00000513596.1:n.*119T>A
ENST00000690831.1:c.*1142T>A (SOX10) ENSP00000510381.1:n.*1142T>A
ENST00000396884.8:c.*119T>A (SOX10) MANE Select ENSP00000380093.2:n.*119T>A
ENST00000651746.1:c.166-2372T>A (SOX10)
ENST00000360880.6:c.*119T>A (SOX10) ENSP00000354130.2:n.*119T>A
ENST00000396884.6:c.*119T>A (SOX10) ENSP00000380093.2:n.*119T>A
ENST00000405557.5:c.293+6206A>T (POLR2F) ENSP00000384112.1:n.293+6206A>T
ENST00000407936.5:c.293+6206A>T (POLR2F) ENSP00000385725.1:n.293+6206A>T
ENST00000443002.5:c.*38+1066A>T (POLR2F) ENSP00000406826.1:n.*38+1066A>T
ENST00000446929.5:c.482+668T>A (SOX10)
NM_001301130.1:c.293+6206A>T (POLR2F) NP_001288059.1:n.293+6206A>T
NM_001301131.1:c.293+6206A>T (POLR2F) NP_001288060.1:n.293+6206A>T
NM_006941.3:c.*119T>A , LRG_271t1:c.*119T>A (SOX10) NP_008872.1:n.*119T>A
XR_938243.1:n.158+1066A>T
NM_001363825.1:c.*38+1066A>T (POLR2F) NP_001350754.1:n.*38+1066A>T
NM_001301130.2:c.293+6206A>T (POLR2F) NP_001288059.1:n.293+6206A>T
NM_001301131.2:c.293+6206A>T (POLR2F) NP_001288060.1:n.293+6206A>T
NM_006941.4:c.*119T>A (SOX10) MANE Select NP_008872.1:n.*119T>A