Canonical Allele Identifier: CA8922858

Gene: CHST9 AQP4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.26916807C>T , CM000680.2:g.26916807C>T	GRCh38
NC_000018.9:g.24496771C>T , CM000680.1:g.24496771C>T	GRCh37
NC_000018.8:g.22750769C>T	NCBI36
NG_029856.1:g.273519G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_031422.6:c.784G>A (CHST9) MANE Select	NP_113610.2:p.Asp262Asn
ENST00000618847.5:c.784G>A (CHST9) MANE Select	ENSP00000480991.1:p.Asp262Asn
NM_001256316.1:c.*521G>A (CHST9)	NP_001243245.1:n.*521G>A
NM_001256316.2:c.*521G>A (CHST9)	NP_001243245.1:n.*521G>A
NM_001398493.1:c.784G>A (CHST9)	NP_001385422.1:p.Asp262Asn
NM_031422.5:c.784G>A (CHST9)	NP_113610.2:p.Asp262Asn
NR_026908.1:n.176-7953C>T (AQP4-AS1)
ENST00000284224.9:c.529G>A (CHST9)	ENSP00000284224.9:p.Asp177Asn
ENST00000580774.2:c.*521G>A (CHST9)	ENSP00000464655.1:n.*521G>A
ENST00000581714.5:c.784G>A (CHST9)	ENSP00000462852.1:p.Asp262Asn
ENST00000618847.4:c.784G>A (CHST9)	ENSP00000480991.1:p.Asp262Asn
XM_005258362.2:c.529G>A (CHST9)	XP_005258419.1:p.Asp177Asn
XM_005258362.4:c.529G>A (CHST9)	XP_005258419.1:p.Asp177Asn
XM_011526224.1:c.613G>A (CHST9)	XP_011524526.1:p.Asp205Asn
XM_011526225.1:c.583G>A (CHST9)	XP_011524527.1:p.Asp195Asn
XM_017026033.1:c.784G>A (CHST9)	XP_016881522.1:p.Asp262Asn
XM_017026034.1:c.613G>A (CHST9)	XP_016881523.1:p.Asp205Asn