Canonical Allele Identifier: CA411497800

Gene: SOX10 POLR2F

Linked Data

• ClinVar Variation Id: 521356
• ClinVar RCV Id: RCV000623200 ; RCV001290177 ; RCV002291283
• dbSNP Id: rs1555938395
• MyVariant Identifiers: chr22:g.38374048G>A (hg19) ; chr22:g.37978041G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37978041G>A , CM000684.2:g.37978041G>A	GRCh38
NC_000022.10:g.38374048G>A , CM000684.1:g.38374048G>A	GRCh37
NC_000022.9:g.36703994G>A	NCBI36
NG_007948.1:g.11492C>T , LRG_271:g.11492C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698177.1:c.739C>T (SOX10)	ENSP00000513596.1:p.Pro247Ser
ENST00000690831.1:c.*145C>T (SOX10)	ENSP00000510381.1:n.*145C>T
ENST00000396884.8:c.523C>T (SOX10) MANE Select	ENSP00000380093.2:p.Pro175Ser
ENST00000360880.6:c.523C>T (SOX10)	ENSP00000354130.2:p.Pro175Ser
ENST00000396884.6:c.523C>T (SOX10)	ENSP00000380093.2:p.Pro175Ser
ENST00000405557.5:c.293+10871G>A (POLR2F)	ENSP00000384112.1:n.293+10871G>A
ENST00000407936.5:c.294-8113G>A (POLR2F)	ENSP00000385725.1:n.294-8113G>A
ENST00000427770.1:c.523C>T (SOX10)	ENSP00000414853.1:p.Pro175Ser
ENST00000443002.5:c.*38+5731G>A (POLR2F)	ENSP00000406826.1:n.*38+5731G>A
ENST00000446929.5:c.153C>T (SOX10)
NM_001301130.1:c.294-8113G>A (POLR2F)	NP_001288059.1:n.294-8113G>A
NM_001301131.1:c.293+10871G>A (POLR2F)	NP_001288060.1:n.293+10871G>A
NM_006941.3:c.523C>T , LRG_271t1:c.523C>T (SOX10)	NP_008872.1:p.Pro175Ser
XR_938243.1:n.158+5731G>A
NM_001363825.1:c.*38+5731G>A (POLR2F)	NP_001350754.1:n.*38+5731G>A
NM_001301130.2:c.294-8113G>A (POLR2F)	NP_001288059.1:n.294-8113G>A
NM_001301131.2:c.293+10871G>A (POLR2F)	NP_001288060.1:n.293+10871G>A
NM_006941.4:c.523C>T (SOX10) MANE Select	NP_008872.1:p.Pro175Ser