Canonical Allele Identifier: CA2404606193

Gene: SOX10 POLR2F

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37983335_37983336delinsCG , CM000684.2:g.37983335_37983336delinsCG	GRCh38
NC_000022.10:g.38379342_38379343delinsCG , CM000684.1:g.38379342_38379343delinsCG	GRCh37
NC_000022.9:g.36709288_36709289delinsCG	NCBI36
NG_007948.1:g.6197_6198delinsCG , LRG_271:g.6197_6198delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698177.1:c.644+21_644+22delinsCG (SOX10)	ENSP00000513596.1:n.644+21_644+22delinsCG
ENST00000690831.1:c.428+21_428+22delinsCG (SOX10)	ENSP00000510381.1:n.428+21_428+22delinsCG
ENST00000396884.8:c.428+21_428+22delinsCG (SOX10) MANE Select	ENSP00000380093.2:n.428+21_428+22delinsCG
ENST00000652356.1:n.738_739delinsCG (SOX10)
ENST00000360880.6:c.428+21_428+22delinsCG (SOX10)	ENSP00000354130.2:n.428+21_428+22delinsCG
ENST00000396884.6:c.428+21_428+22delinsCG (SOX10)	ENSP00000380093.2:n.428+21_428+22delinsCG
ENST00000405557.5:c.293+16165_293+16166delinsCG (POLR2F)	ENSP00000384112.1:n.293+16165_293+16166delinsCG
ENST00000407936.5:c.294-2819_294-2818delinsCG (POLR2F)	ENSP00000385725.1:n.294-2819_294-2818delinsCG
ENST00000427770.1:c.428+21_428+22delinsCG (SOX10)	ENSP00000414853.1:n.428+21_428+22delinsCG
ENST00000443002.5:c.*39-1717_*39-1716delinsCG (POLR2F)	ENSP00000406826.1:n.*39-1717_*39-1716delinsCG
ENST00000446929.5:c.58+21_58+22delinsCG (SOX10)
ENST00000470555.1:n.70+1003_70+1004delinsCG (SOX10)
NM_001301130.1:c.294-2819_294-2818delinsCG (POLR2F)	NP_001288059.1:n.294-2819_294-2818delinsCG
NM_001301131.1:c.293+16165_293+16166delinsCG (POLR2F)	NP_001288060.1:n.293+16165_293+16166delinsCG
NM_006941.3:c.428+21_428+22delinsCG , LRG_271t1:c.428+21_428+22delinsCG (SOX10)	NP_008872.1:n.428+21_428+22delinsCG
XR_938243.1:n.158+11025_158+11026delinsCG
NM_001363825.1:c.*38+11025_*38+11026delinsCG (POLR2F)	NP_001350754.1:n.*38+11025_*38+11026delinsCG
NM_001301130.2:c.294-2819_294-2818delinsCG (POLR2F)	NP_001288059.1:n.294-2819_294-2818delinsCG
NM_001301131.2:c.293+16165_293+16166delinsCG (POLR2F)	NP_001288060.1:n.293+16165_293+16166delinsCG
NM_006941.4:c.428+21_428+22delinsCG (SOX10) MANE Select	NP_008872.1:n.428+21_428+22delinsCG