Canonical Allele Identifier: CA2404602274

Gene: SOX10 POLR2F

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37974148G= , CM000684.2:g.37974148G=	GRCh38
NC_000022.10:g.38370155G= , CM000684.1:g.38370155G=	GRCh37
NC_000022.9:g.36700101G=	NCBI36
NG_007948.1:g.15385C= , LRG_271:g.15385C=

Transcript Alleles

HGVS	Amino-acid Change
NM_006941.4:c.748C= (SOX10) MANE Select	NP_008872.1:p.Gln250=
ENST00000396884.8:c.748C= (SOX10) MANE Select	ENSP00000380093.2:p.Gln250=
NM_001301130.1:c.293+6978G= (POLR2F)	NP_001288059.1:n.293+6978G=
NM_001301130.2:c.293+6978G= (POLR2F)	NP_001288059.1:n.293+6978G=
NM_001301131.1:c.293+6978G= (POLR2F)	NP_001288060.1:n.293+6978G=
NM_001301131.2:c.293+6978G= (POLR2F)	NP_001288060.1:n.293+6978G=
NM_001363825.1:c.*38+1838G= (POLR2F)	NP_001350754.1:n.*38+1838G=
NM_006941.3:c.748C= , LRG_271t1:c.748C= (SOX10)	NP_008872.1:p.Gln250=
ENST00000360880.6:c.748C= (SOX10)	ENSP00000354130.2:p.Gln250=
ENST00000396884.6:c.748C= (SOX10)	ENSP00000380093.2:p.Gln250=
ENST00000405557.5:c.293+6978G= (POLR2F)	ENSP00000384112.1:n.293+6978G=
ENST00000407936.5:c.293+6978G= (POLR2F)	ENSP00000385725.1:n.293+6978G=
ENST00000443002.5:c.*38+1838G= (POLR2F)	ENSP00000406826.1:n.*38+1838G=
ENST00000446929.5:c.378C= (SOX10)
ENST00000651746.1:c.166-3144C= (SOX10)
ENST00000690831.1:c.*370C= (SOX10)	ENSP00000510381.1:n.*370C=
ENST00000698177.1:c.964C= (SOX10)	ENSP00000513596.1:p.Gln322=
XR_938243.1:n.158+1838G=