Canonical Allele Identifier: CA411491434

Gene: SOX10 POLR2F

Linked Data

• gnomAD v4: 22-37973842-C-T
• MyVariant Identifiers: chr22:g.38369849C>T (hg19) ; chr22:g.37973842C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37973842C>T , CM000684.2:g.37973842C>T	GRCh38
NC_000022.10:g.38369849C>T , CM000684.1:g.38369849C>T	GRCh37
NC_000022.9:g.36699795C>T	NCBI36
NG_007948.1:g.15691G>A , LRG_271:g.15691G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698177.1:c.1270G>A (SOX10)	ENSP00000513596.1:p.Ala424Thr
ENST00000690831.1:c.*676G>A (SOX10)	ENSP00000510381.1:n.*676G>A
ENST00000396884.8:c.1054G>A (SOX10) MANE Select	ENSP00000380093.2:p.Ala352Thr
ENST00000651746.1:c.166-2838G>A (SOX10)
ENST00000360880.6:c.1054G>A (SOX10)	ENSP00000354130.2:p.Ala352Thr
ENST00000396884.6:c.1054G>A (SOX10)	ENSP00000380093.2:p.Ala352Thr
ENST00000405557.5:c.293+6672C>T (POLR2F)	ENSP00000384112.1:n.293+6672C>T
ENST00000407936.5:c.293+6672C>T (POLR2F)	ENSP00000385725.1:n.293+6672C>T
ENST00000443002.5:c.*38+1532C>T (POLR2F)	ENSP00000406826.1:n.*38+1532C>T
ENST00000446929.5:c.482+202G>A (SOX10)
NM_001301130.1:c.293+6672C>T (POLR2F)	NP_001288059.1:n.293+6672C>T
NM_001301131.1:c.293+6672C>T (POLR2F)	NP_001288060.1:n.293+6672C>T
NM_006941.3:c.1054G>A , LRG_271t1:c.1054G>A (SOX10)	NP_008872.1:p.Ala352Thr
XR_938243.1:n.158+1532C>T
NM_001363825.1:c.*38+1532C>T (POLR2F)	NP_001350754.1:n.*38+1532C>T
NM_001301130.2:c.293+6672C>T (POLR2F)	NP_001288059.1:n.293+6672C>T
NM_001301131.2:c.293+6672C>T (POLR2F)	NP_001288060.1:n.293+6672C>T
NM_006941.4:c.1054G>A (SOX10) MANE Select	NP_008872.1:p.Ala352Thr