Canonical Allele Identifier: CA2273925868
Gene: SOX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122712_72122713delinsCG , CM000679.2:g.72122712_72122713delinsCG GRCh38
NC_000017.10:g.70118853_70118854delinsCG , CM000679.1:g.70118853_70118854delinsCG GRCh37
NC_000017.9:g.67630448_67630449delinsCG NCBI36
NG_012490.1:g.6693_6694delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.432-7_432-6delinsCG MANE Select ENSP00000245479.2:n.432-7_432-6delinsCG
ENST00000245479.2:c.432-7_432-6delinsCG ENSP00000245479.2:n.432-7_432-6delinsCG
NM_000346.3:c.432-7_432-6delinsCG NP_000337.1:n.432-7_432-6delinsCG
NM_000346.4:c.432-7_432-6delinsCG MANE Select NP_000337.1:n.432-7_432-6delinsCG