Canonical Allele Identifier: CA2273926248
Gene: SOX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123421_72123422delinsGC , CM000679.2:g.72123421_72123422delinsGC GRCh38
NC_000017.10:g.70119562_70119563delinsGC , CM000679.1:g.70119562_70119563delinsGC GRCh37
NC_000017.9:g.67631157_67631158delinsGC NCBI36
NG_012490.1:g.7402_7403delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.686-122_686-121delinsGC MANE Select ENSP00000245479.2:n.686-122_686-121delinsGC
ENST00000245479.2:c.686-122_686-121delinsGC ENSP00000245479.2:n.686-122_686-121delinsGC
NM_000346.3:c.686-122_686-121delinsGC NP_000337.1:n.686-122_686-121delinsGC
NM_000346.4:c.686-122_686-121delinsGC MANE Select NP_000337.1:n.686-122_686-121delinsGC