Canonical Allele Identifier: CA644626142
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 436774
ClinVar RCV Id: RCV000501576 RCV001461996
dbSNP Id: rs1556623179
gnomAD v2: X-135126605-A-G
gnomAD v4: X-136044446-A-G
MyVariant Identifiers: chrX:g.135126605A>G (hg19) chrX:g.136044446A>G (hg38)
ERepo: CA644626142/MONDO:0010278/033
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136044446A>G , CM000685.2:g.136044446A>G GRCh38
NC_000023.10:g.135126605A>G , CM000685.1:g.135126605A>G GRCh37
NC_000023.9:g.134954271A>G NCBI36
NG_017160.1:g.64020A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370695.8:c.1834-6A>G ENSP00000359729.4:n.1834-6A>G
ENST00000370701.6:c.1678-6A>G ENSP00000359735.1:n.1678-6A>G
ENST00000630721.3:c.1768-6A>G MANE Select ENSP00000487486.2:n.1768-6A>G
ENST00000636092.1:c.1678-6A>G ENSP00000490406.1:n.1678-6A>G
ENST00000636206.2:n.1008-6A>G
ENST00000636347.1:c.1678-6A>G ENSP00000490648.1:n.1678-6A>G
ENST00000636625.1:n.669-6A>G
ENST00000636798.1:n.1113-6A>G
ENST00000637195.1:c.1582-6A>G ENSP00000490330.1:n.1582-6A>G
ENST00000637234.1:c.1678-6A>G ENSP00000490527.1:n.1678-6A>G
ENST00000637581.1:c.1678-6A>G ENSP00000490731.1:n.1678-6A>G
ENST00000676233.1:n.1001-6A>G
ENST00000678163.1:c.1924-6A>G ENSP00000502845.1:n.1924-6A>G
ENST00000370695.6:c.1834-6A>G ENSP00000359729.4:n.1834-6A>G
ENST00000370698.7:c.1738-6A>G ENSP00000359732.3:n.1738-6A>G
ENST00000370701.5:c.1678-6A>G ENSP00000359735.1:n.1678-6A>G
ENST00000626147.1:n.567-6A>G
ENST00000630721.1:c.414-6A>G
NM_001042537.1:c.1834-6A>G NP_001036002.1:n.1834-6A>G
NM_001177651.1:c.1678-6A>G NP_001171122.1:n.1678-6A>G
NM_006359.2:c.1738-6A>G NP_006350.1:n.1738-6A>G
XM_006724726.2:c.1678-6A>G XP_006724789.1:n.1678-6A>G
XM_011531243.1:c.1582-6A>G XP_011529545.1:n.1582-6A>G
NM_001330652.1:c.1582-6A>G NP_001317581.1:n.1582-6A>G
XM_006724726.3:c.1678-6A>G XP_006724789.1:n.1678-6A>G
XM_017029223.2:c.1678-6A>G XP_016884712.1:n.1678-6A>G
XM_017029224.1:c.1678-6A>G XP_016884713.1:n.1678-6A>G
XM_017029225.1:c.1582-6A>G XP_016884714.1:n.1582-6A>G
NM_001177651.2:c.1678-6A>G NP_001171122.1:n.1678-6A>G
NM_001330652.2:c.1582-6A>G NP_001317581.1:n.1582-6A>G
NM_006359.3:c.1738-6A>G NP_006350.1:n.1738-6A>G
NM_001042537.2:c.1834-6A>G NP_001036002.1:n.1834-6A>G
NM_001379110.1:c.1768-6A>G MANE Select NP_001366039.1:n.1768-6A>G
NM_001400909.1:c.1678-6A>G NP_001387838.1:n.1678-6A>G
NM_001400910.1:c.1678-6A>G NP_001387839.1:n.1678-6A>G
NM_001400911.1:c.1678-6A>G NP_001387840.1:n.1678-6A>G
NM_001400912.1:c.1678-6A>G NP_001387841.1:n.1678-6A>G
NM_001400913.1:c.1582-6A>G NP_001387842.1:n.1582-6A>G
Search 100 bp 5'
Search 100 bp 3'