Canonical Allele Identifier: CA2291705318

Gene: CHST9

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.26990638T= , CM000680.2:g.26990638T=	GRCh38
NC_000018.9:g.24570602T= , CM000680.1:g.24570602T=	GRCh37
NC_000018.8:g.22824600T=	NCBI36
NG_029856.1:g.199688A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000618847.5:c.202+33478A= MANE Select	ENSP00000480991.1:n.202+33478A=
ENST00000284224.9:c.-16+33478A=	ENSP00000284224.9:n.-16+33478A=
ENST00000580774.2:c.202+33478A=	ENSP00000464655.1:n.202+33478A=
ENST00000581714.5:c.202+33478A=	ENSP00000462852.1:n.202+33478A=
ENST00000618847.4:c.202+33478A=	ENSP00000480991.1:n.202+33478A=
NM_001256316.1:c.202+33478A=	NP_001243245.1:n.202+33478A=
NM_031422.5:c.202+33478A=	NP_113610.2:n.202+33478A=
XM_006722555.2:c.202+33478A=	XP_006722618.1:n.202+33478A=
XM_011526225.1:c.1+33478A=	XP_011524527.1:n.1+33478A=
XM_006722555.4:c.202+33478A=	XP_006722618.1:n.202+33478A=
XM_017026033.1:c.202+33478A=	XP_016881522.1:n.202+33478A=
XM_017026034.1:c.-66-11886A=	XP_016881523.1:n.-66-11886A=
NM_031422.6:c.202+33478A= MANE Select	NP_113610.2:n.202+33478A=
NM_001256316.2:c.202+33478A=	NP_001243245.1:n.202+33478A=
NM_001398493.1:c.202+33478A=	NP_001385422.1:n.202+33478A=