Canonical Allele Identifier: CA2273925768
Gene: SOX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122515_72122516delinsGT , CM000679.2:g.72122515_72122516delinsGT GRCh38
NC_000017.10:g.70118656_70118657delinsGT , CM000679.1:g.70118656_70118657delinsGT GRCh37
NC_000017.9:g.67630251_67630252delinsGT NCBI36
NG_012490.1:g.6496_6497delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.432-204_432-203delinsGT MANE Select ENSP00000245479.2:n.432-204_432-203delinsGT
ENST00000245479.2:c.432-204_432-203delinsGT ENSP00000245479.2:n.432-204_432-203delinsGT
NM_000346.3:c.432-204_432-203delinsGT NP_000337.1:n.432-204_432-203delinsGT
NM_000346.4:c.432-204_432-203delinsGT MANE Select NP_000337.1:n.432-204_432-203delinsGT