Canonical Allele Identifier: CA414606849
Gene: SLC9A6 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135067915T>C (hg19) chrX:g.135985756T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.135985756T>C , CM000685.2:g.135985756T>C GRCh38
NC_000023.10:g.135067915T>C , CM000685.1:g.135067915T>C GRCh37
NC_000023.9:g.134895581T>C NCBI36
NG_017160.1:g.5330T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370695.8:c.254T>C ENSP00000359729.4:p.Ile85Thr
ENST00000370701.6:c.98T>C ENSP00000359735.1:p.Ile33Thr
ENST00000630721.3:c.98T>C MANE Select ENSP00000487486.2:p.Ile33Thr
ENST00000636092.1:c.98T>C ENSP00000490406.1:p.Ile33Thr
ENST00000636347.1:c.98T>C ENSP00000490648.1:p.Ile33Thr
ENST00000637195.1:c.98T>C ENSP00000490330.1:p.Ile33Thr
ENST00000637234.1:c.98T>C ENSP00000490527.1:p.Ile33Thr
ENST00000637581.1:c.98T>C ENSP00000490731.1:p.Ile33Thr
ENST00000643775.1:n.41T>C
ENST00000674809.1:c.41T>C ENSP00000502455.1:p.Ile14Thr
ENST00000675550.1:n.39T>C
ENST00000675856.1:n.41T>C
ENST00000676043.1:c.41T>C ENSP00000501920.1:p.Ile14Thr
ENST00000678163.1:c.254T>C ENSP00000502845.1:p.Ile85Thr
ENST00000370695.6:c.254T>C ENSP00000359729.4:p.Ile85Thr
ENST00000370698.7:c.254T>C ENSP00000359732.3:p.Ile85Thr
ENST00000370701.5:c.98T>C ENSP00000359735.1:p.Ile33Thr
ENST00000627534.2:c.98T>C ENSP00000486743.1:p.Ile33Thr
NM_001042537.1:c.254T>C NP_001036002.1:p.Ile85Thr
NM_001177651.1:c.98T>C NP_001171122.1:p.Ile33Thr
NM_006359.2:c.254T>C NP_006350.1:p.Ile85Thr
XM_006724726.2:c.98T>C XP_006724789.1:p.Ile33Thr
XM_011531243.1:c.98T>C XP_011529545.1:p.Ile33Thr
NM_001330652.1:c.98T>C NP_001317581.1:p.Ile33Thr
XM_006724726.3:c.98T>C XP_006724789.1:p.Ile33Thr
XM_017029223.2:c.98T>C XP_016884712.1:p.Ile33Thr
XM_017029224.1:c.98T>C XP_016884713.1:p.Ile33Thr
XM_017029225.1:c.98T>C XP_016884714.1:p.Ile33Thr
NM_001177651.2:c.98T>C NP_001171122.1:p.Ile33Thr
NM_001330652.2:c.98T>C NP_001317581.1:p.Ile33Thr
NM_006359.3:c.254T>C NP_006350.1:p.Ile85Thr
NM_001042537.2:c.254T>C NP_001036002.1:p.Ile85Thr
NM_001379110.1:c.98T>C MANE Select NP_001366039.1:p.Ile33Thr
NM_001400909.1:c.98T>C NP_001387838.1:p.Ile33Thr
NM_001400910.1:c.98T>C NP_001387839.1:p.Ile33Thr
NM_001400911.1:c.98T>C NP_001387840.1:p.Ile33Thr
NM_001400912.1:c.98T>C NP_001387841.1:p.Ile33Thr
NM_001400913.1:c.98T>C NP_001387842.1:p.Ile33Thr
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