Canonical Allele Identifier: CA645598914
Gene: SOX9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123600_72123601dup , CM000679.2:g.72123600_72123601dup GRCh38
NC_000017.10:g.70119741_70119742dup , CM000679.1:g.70119741_70119742dup GRCh37
NC_000017.9:g.67631336_67631337dup NCBI36
NG_012490.1:g.7581_7582dup

Transcript Alleles

HGVS Amino-acid change
ENST00000245479.3:c.743_744dup MANE Select ENSP00000245479.2:p.Lys249AlafsTer5
ENST00000245479.2:c.743_744dup ENSP00000245479.2:p.Lys249AlafsTer5
NM_000346.3:c.743_744dup NP_000337.1:p.Lys249AlafsTer5
NM_000346.4:c.743_744dup MANE Select NP_000337.1:p.Lys249AlafsTer5