Canonical Allele Identifier: CA2639603163
Gene: SOX9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123931_72123972del , CM000679.2:g.72123931_72123972del GRCh38
NC_000017.10:g.70120072_70120113del , CM000679.1:g.70120072_70120113del GRCh37
NC_000017.9:g.67631667_67631708del NCBI36
NG_012490.1:g.7912_7953del

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.1074_1115del MANE Select ENSP00000245479.2:p.Pro359_Ala372del
ENST00000245479.2:c.1074_1115del ENSP00000245479.2:p.Pro359_Ala372del
NM_000346.3:c.1074_1115del NP_000337.1:p.Pro359_Ala372del
NM_000346.4:c.1074_1115del MANE Select NP_000337.1:p.Pro359_Ala372del