Canonical Allele Identifier: CA2273925745
Gene: SOX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122491_72122492delinsAG , CM000679.2:g.72122491_72122492delinsAG GRCh38
NC_000017.10:g.70118632_70118633delinsAG , CM000679.1:g.70118632_70118633delinsAG GRCh37
NC_000017.9:g.67630227_67630228delinsAG NCBI36
NG_012490.1:g.6472_6473delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.432-228_432-227delinsAG MANE Select ENSP00000245479.2:n.432-228_432-227delinsAG
ENST00000245479.2:c.432-228_432-227delinsAG ENSP00000245479.2:n.432-228_432-227delinsAG
NM_000346.3:c.432-228_432-227delinsAG NP_000337.1:n.432-228_432-227delinsAG
NM_000346.4:c.432-228_432-227delinsAG MANE Select NP_000337.1:n.432-228_432-227delinsAG