Canonical Allele Identifier: CA627589917
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs1177636054

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72124038_72124043del , CM000679.2:g.72124038_72124043del GRCh38
NC_000017.10:g.70120179_70120184del , CM000679.1:g.70120179_70120184del GRCh37
NC_000017.9:g.67631774_67631779del NCBI36
NG_012490.1:g.8019_8024del

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.1181_1186del MANE Select ENSP00000245479.2:p.Arg394_Thr395del
ENST00000245479.2:c.1181_1186del ENSP00000245479.2:p.Arg394_Thr395del
NM_000346.3:c.1181_1186del NP_000337.1:p.Arg394_Thr395del
NM_000346.4:c.1181_1186del MANE Select NP_000337.1:p.Arg394_Thr395del