Canonical Allele Identifier: CA10524775

Gene: SLC9A6

Linked Data

• ClinVar Variation Id: 1052390
• ClinVar RCV Id: RCV001360563
• dbSNP Id: rs782772247
• ExAC: X:135098880 A / G
• gnomAD v2: X-135098880-A-G
• gnomAD v3: X-136016721-A-G
• gnomAD v4: X-136016721-A-G
• MyVariant Identifiers: chrX:g.135098880A>G (hg19) ; chrX:g.136016721A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136016721A>G , CM000685.2:g.136016721A>G	GRCh38
NC_000023.10:g.135098880A>G , CM000685.1:g.135098880A>G	GRCh37
NC_000023.9:g.134926546A>G	NCBI36
NG_017160.1:g.36295A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370695.8:c.1313A>G	ENSP00000359729.4:p.Asn438Ser
ENST00000370701.6:c.1157A>G	ENSP00000359735.1:p.Asn386Ser
ENST00000630721.3:c.1157A>G MANE Select	ENSP00000487486.2:p.Asn386Ser
ENST00000636092.1:c.1157A>G	ENSP00000490406.1:p.Asn386Ser
ENST00000636347.1:c.1157A>G	ENSP00000490648.1:p.Asn386Ser
ENST00000636798.1:n.592A>G
ENST00000637195.1:c.1061A>G	ENSP00000490330.1:p.Asn354Ser
ENST00000637234.1:c.1157A>G	ENSP00000490527.1:p.Asn386Ser
ENST00000637581.1:c.1157A>G	ENSP00000490731.1:p.Asn386Ser
ENST00000643775.1:n.1100A>G
ENST00000675856.1:n.1100A>G
ENST00000678163.1:c.1313A>G	ENSP00000502845.1:p.Asn438Ser
ENST00000370695.6:c.1313A>G	ENSP00000359729.4:p.Asn438Ser
ENST00000370698.7:c.1217A>G	ENSP00000359732.3:p.Asn406Ser
ENST00000370701.5:c.1157A>G	ENSP00000359735.1:p.Asn386Ser
NM_001042537.1:c.1313A>G	NP_001036002.1:p.Asn438Ser
NM_001177651.1:c.1157A>G	NP_001171122.1:p.Asn386Ser
NM_006359.2:c.1217A>G	NP_006350.1:p.Asn406Ser
XM_006724726.2:c.1157A>G	XP_006724789.1:p.Asn386Ser
XM_011531243.1:c.1061A>G	XP_011529545.1:p.Asn354Ser
NM_001330652.1:c.1061A>G	NP_001317581.1:p.Asn354Ser
XM_006724726.3:c.1157A>G	XP_006724789.1:p.Asn386Ser
XM_017029223.2:c.1157A>G	XP_016884712.1:p.Asn386Ser
XM_017029224.1:c.1157A>G	XP_016884713.1:p.Asn386Ser
XM_017029225.1:c.1061A>G	XP_016884714.1:p.Asn354Ser
NM_001177651.2:c.1157A>G	NP_001171122.1:p.Asn386Ser
NM_001330652.2:c.1061A>G	NP_001317581.1:p.Asn354Ser
NM_006359.3:c.1217A>G	NP_006350.1:p.Asn406Ser
NM_001042537.2:c.1313A>G	NP_001036002.1:p.Asn438Ser
NM_001379110.1:c.1157A>G MANE Select	NP_001366039.1:p.Asn386Ser
NM_001400909.1:c.1157A>G	NP_001387838.1:p.Asn386Ser
NM_001400910.1:c.1157A>G	NP_001387839.1:p.Asn386Ser
NM_001400911.1:c.1157A>G	NP_001387840.1:p.Asn386Ser
NM_001400912.1:c.1157A>G	NP_001387841.1:p.Asn386Ser
NM_001400913.1:c.1061A>G	NP_001387842.1:p.Asn354Ser