Canonical Allele Identifier: CA2273925843
Gene: SOX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122676_72122677delinsCT , CM000679.2:g.72122676_72122677delinsCT GRCh38
NC_000017.10:g.70118817_70118818delinsCT , CM000679.1:g.70118817_70118818delinsCT GRCh37
NC_000017.9:g.67630412_67630413delinsCT NCBI36
NG_012490.1:g.6657_6658delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.432-43_432-42delinsCT MANE Select ENSP00000245479.2:n.432-43_432-42delinsCT
ENST00000245479.2:c.432-43_432-42delinsCT ENSP00000245479.2:n.432-43_432-42delinsCT
NM_000346.3:c.432-43_432-42delinsCT NP_000337.1:n.432-43_432-42delinsCT
NM_000346.4:c.432-43_432-42delinsCT MANE Select NP_000337.1:n.432-43_432-42delinsCT