Canonical Allele Identifier: CA345865864

Gene: SOX11

Linked Data

• COSMIC: COSM4094943
• MyVariant Identifiers: chr2:g.5832927A>C (hg19) ; chr2:g.5692795A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.5692795A>C , CM000664.2:g.5692795A>C	GRCh38
NC_000002.11:g.5832927A>C , CM000664.1:g.5832927A>C	GRCh37
NC_000002.10:g.5750378A>C	NCBI36
NG_050751.1:g.5129A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322002.5:c.74A>C MANE Select	ENSP00000322568.3:p.Glu25Ala
ENST00000322002.4:c.74A>C	ENSP00000322568.3:p.Glu25Ala
NM_003108.3:c.74A>C	NP_003099.1:p.Glu25Ala
NM_003108.4:c.74A>C MANE Select	NP_003099.1:p.Glu25Ala