Canonical Allele Identifier: CA2810344922

Gene: SOX9

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.72122452_72122453insAAAA , CM000679.2:g.72122452_72122453insAAAA	GRCh38
NC_000017.10:g.70118593_70118594insAAAA , CM000679.1:g.70118593_70118594insAAAA	GRCh37
NC_000017.9:g.67630188_67630189insAAAA	NCBI36
NG_012490.1:g.6433_6434insAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245479.3:c.432-267_432-266insAAAA MANE Select	ENSP00000245479.2:n.432-267_432-266insAAAA
ENST00000245479.2:c.432-267_432-266insAAAA	ENSP00000245479.2:n.432-267_432-266insAAAA
NM_000346.3:c.432-267_432-266insAAAA	NP_000337.1:n.432-267_432-266insAAAA
NM_000346.4:c.432-267_432-266insAAAA MANE Select	NP_000337.1:n.432-267_432-266insAAAA