Canonical Allele Identifier: CA345865864
Gene: SOX11 HGNC NCBI

Linked Data

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