Canonical Allele Identifier: CA2404603804

Gene: SOX10 POLR2F

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37977942T= , CM000684.2:g.37977942T=	GRCh38
NC_000022.10:g.38373949T= , CM000684.1:g.38373949T=	GRCh37
NC_000022.9:g.36703895T=	NCBI36
NG_007948.1:g.11591A= , LRG_271:g.11591A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698177.1:c.838A= (SOX10)	ENSP00000513596.1:p.Lys280=
ENST00000690831.1:c.*244A= (SOX10)	ENSP00000510381.1:n.*244A=
ENST00000396884.8:c.622A= (SOX10) MANE Select	ENSP00000380093.2:p.Lys208=
ENST00000651746.1:c.90A= (SOX10)
ENST00000360880.6:c.622A= (SOX10)	ENSP00000354130.2:p.Lys208=
ENST00000396884.6:c.622A= (SOX10)	ENSP00000380093.2:p.Lys208=
ENST00000405557.5:c.293+10772T= (POLR2F)	ENSP00000384112.1:n.293+10772T=
ENST00000407936.5:c.294-8212T= (POLR2F)	ENSP00000385725.1:n.294-8212T=
ENST00000427770.1:c.622A= (SOX10)	ENSP00000414853.1:p.Lys208=
ENST00000443002.5:c.*38+5632T= (POLR2F)	ENSP00000406826.1:n.*38+5632T=
ENST00000446929.5:c.252A= (SOX10)
NM_001301130.1:c.294-8212T= (POLR2F)	NP_001288059.1:n.294-8212T=
NM_001301131.1:c.293+10772T= (POLR2F)	NP_001288060.1:n.293+10772T=
NM_006941.3:c.622A= , LRG_271t1:c.622A= (SOX10)	NP_008872.1:p.Lys208=
XR_938243.1:n.158+5632T=
NM_001363825.1:c.*38+5632T= (POLR2F)	NP_001350754.1:n.*38+5632T=
NM_001301130.2:c.294-8212T= (POLR2F)	NP_001288059.1:n.294-8212T=
NM_001301131.2:c.293+10772T= (POLR2F)	NP_001288060.1:n.293+10772T=
NM_006941.4:c.622A= (SOX10) MANE Select	NP_008872.1:p.Lys208=