Canonical Allele Identifier: CA411491211

Gene: SOX10 POLR2F

Linked Data

• gnomAD v4: 22-37973823-G-A
• MyVariant Identifiers: chr22:g.38369830G>A (hg19) ; chr22:g.37973823G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37973823G>A , CM000684.2:g.37973823G>A	GRCh38
NC_000022.10:g.38369830G>A , CM000684.1:g.38369830G>A	GRCh37
NC_000022.9:g.36699776G>A	NCBI36
NG_007948.1:g.15710C>T , LRG_271:g.15710C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698177.1:c.1289C>T (SOX10)	ENSP00000513596.1:p.Thr430Ile
ENST00000690831.1:c.*695C>T (SOX10)	ENSP00000510381.1:n.*695C>T
ENST00000396884.8:c.1073C>T (SOX10) MANE Select	ENSP00000380093.2:p.Thr358Ile
ENST00000651746.1:c.166-2819C>T (SOX10)
ENST00000360880.6:c.1073C>T (SOX10)	ENSP00000354130.2:p.Thr358Ile
ENST00000396884.6:c.1073C>T (SOX10)	ENSP00000380093.2:p.Thr358Ile
ENST00000405557.5:c.293+6653G>A (POLR2F)	ENSP00000384112.1:n.293+6653G>A
ENST00000407936.5:c.293+6653G>A (POLR2F)	ENSP00000385725.1:n.293+6653G>A
ENST00000443002.5:c.*38+1513G>A (POLR2F)	ENSP00000406826.1:n.*38+1513G>A
ENST00000446929.5:c.482+221C>T (SOX10)
NM_001301130.1:c.293+6653G>A (POLR2F)	NP_001288059.1:n.293+6653G>A
NM_001301131.1:c.293+6653G>A (POLR2F)	NP_001288060.1:n.293+6653G>A
NM_006941.3:c.1073C>T , LRG_271t1:c.1073C>T (SOX10)	NP_008872.1:p.Thr358Ile
XR_938243.1:n.158+1513G>A
NM_001363825.1:c.*38+1513G>A (POLR2F)	NP_001350754.1:n.*38+1513G>A
NM_001301130.2:c.293+6653G>A (POLR2F)	NP_001288059.1:n.293+6653G>A
NM_001301131.2:c.293+6653G>A (POLR2F)	NP_001288060.1:n.293+6653G>A
NM_006941.4:c.1073C>T (SOX10) MANE Select	NP_008872.1:p.Thr358Ile