Canonical Allele Identifier: CA645598833
Gene: SOX9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72124042_72124043dup , CM000679.2:g.72124042_72124043dup GRCh38
NC_000017.10:g.70120183_70120184dup , CM000679.1:g.70120183_70120184dup GRCh37
NC_000017.9:g.67631778_67631779dup NCBI36
NG_012490.1:g.8023_8024dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.1185_1186dup MANE Select ENSP00000245479.2:p.His396ArgfsTer8
ENST00000245479.2:c.1185_1186dup ENSP00000245479.2:p.His396ArgfsTer8
NM_000346.3:c.1185_1186dup NP_000337.1:p.His396ArgfsTer8
NM_000346.4:c.1185_1186dup MANE Select NP_000337.1:p.His396ArgfsTer8