Canonical Allele Identifier: CA2810344911
Gene: SOX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122446_72122447insAAAAAA , CM000679.2:g.72122446_72122447insAAAAAA GRCh38
NC_000017.10:g.70118587_70118588insAAAAAA , CM000679.1:g.70118587_70118588insAAAAAA GRCh37
NC_000017.9:g.67630182_67630183insAAAAAA NCBI36
NG_012490.1:g.6427_6428insAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.432-273_432-272insAAAAAA MANE Select ENSP00000245479.2:n.432-273_432-272insAAAAAA
ENST00000245479.2:c.432-273_432-272insAAAAAA ENSP00000245479.2:n.432-273_432-272insAAAAAA
NM_000346.3:c.432-273_432-272insAAAAAA NP_000337.1:n.432-273_432-272insAAAAAA
NM_000346.4:c.432-273_432-272insAAAAAA MANE Select NP_000337.1:n.432-273_432-272insAAAAAA