Canonical Allele Identifier: CA2639603100
Gene: SOX9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123510_72123511insACA , CM000679.2:g.72123510_72123511insACA GRCh38
NC_000017.10:g.70119651_70119652insACA , CM000679.1:g.70119651_70119652insACA GRCh37
NC_000017.9:g.67631246_67631247insACA NCBI36
NG_012490.1:g.7491_7492insACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.686-33_686-32insACA MANE Select ENSP00000245479.2:n.686-33_686-32insACA
ENST00000245479.2:c.686-33_686-32insACA ENSP00000245479.2:n.686-33_686-32insACA
NM_000346.3:c.686-33_686-32insACA NP_000337.1:n.686-33_686-32insACA
NM_000346.4:c.686-33_686-32insACA MANE Select NP_000337.1:n.686-33_686-32insACA