Canonical Allele Identifier: CA2503392470
Gene: SLC9A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.135998501_135998502insAAAAAGGA , CM000685.2:g.135998501_135998502insAAAAAGGA GRCh38
NC_000023.10:g.135080660_135080661insAAAAAGGA , CM000685.1:g.135080660_135080661insAAAAAGGA GRCh37
NC_000023.9:g.134908326_134908327insAAAAAGGA NCBI36
NG_017160.1:g.18075_18076insAAAAAGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000370695.8:c.623_624insAAAAAGGA ENSP00000359729.4:p.Gly209LysfsTer7
ENST00000370701.6:c.467_468insAAAAAGGA ENSP00000359735.1:p.Gly157LysfsTer7
ENST00000630721.3:c.467_468insAAAAAGGA MANE Select ENSP00000487486.2:p.Gly157LysfsTer7
ENST00000636092.1:c.467_468insAAAAAGGA ENSP00000490406.1:p.Gly157LysfsTer7
ENST00000636347.1:c.467_468insAAAAAGGA ENSP00000490648.1:p.Gly157LysfsTer7
ENST00000637195.1:c.371_372insAAAAAGGA ENSP00000490330.1:p.Gly125LysfsTer7
ENST00000637234.1:c.467_468insAAAAAGGA ENSP00000490527.1:p.Gly157LysfsTer7
ENST00000637581.1:c.467_468insAAAAAGGA ENSP00000490731.1:p.Gly157LysfsTer7
ENST00000643775.1:n.410_411insAAAAAGGA
ENST00000674809.1:c.410_411insAAAAAGGA ENSP00000502455.1:p.Gly138LysfsTer7
ENST00000675550.1:n.408_409insAAAAAGGA
ENST00000675856.1:n.410_411insAAAAAGGA
ENST00000676043.1:c.410_411insAAAAAGGA ENSP00000501920.1:p.Gly138LysfsTer7
ENST00000678163.1:c.623_624insAAAAAGGA ENSP00000502845.1:p.Gly209LysfsTer7
ENST00000370695.6:c.623_624insAAAAAGGA ENSP00000359729.4:p.Gly209LysfsTer7
ENST00000370698.7:c.527_528insAAAAAGGA ENSP00000359732.3:p.Gly177LysfsTer7
ENST00000370701.5:c.467_468insAAAAAGGA ENSP00000359735.1:p.Gly157LysfsTer7
ENST00000627534.2:c.467_468insAAAAAGGA ENSP00000486743.1:p.Gly157LysfsTer7
NM_001042537.1:c.623_624insAAAAAGGA NP_001036002.1:p.Gly209LysfsTer7
NM_001177651.1:c.467_468insAAAAAGGA NP_001171122.1:p.Gly157LysfsTer7
NM_006359.2:c.527_528insAAAAAGGA NP_006350.1:p.Gly177LysfsTer7
XM_006724726.2:c.467_468insAAAAAGGA XP_006724789.1:p.Gly157LysfsTer7
XM_011531243.1:c.371_372insAAAAAGGA XP_011529545.1:p.Gly125LysfsTer7
NM_001330652.1:c.371_372insAAAAAGGA NP_001317581.1:p.Gly125LysfsTer7
XM_006724726.3:c.467_468insAAAAAGGA XP_006724789.1:p.Gly157LysfsTer7
XM_017029223.2:c.467_468insAAAAAGGA XP_016884712.1:p.Gly157LysfsTer7
XM_017029224.1:c.467_468insAAAAAGGA XP_016884713.1:p.Gly157LysfsTer7
XM_017029225.1:c.371_372insAAAAAGGA XP_016884714.1:p.Gly125LysfsTer7
NM_001177651.2:c.467_468insAAAAAGGA NP_001171122.1:p.Gly157LysfsTer7
NM_001330652.2:c.371_372insAAAAAGGA NP_001317581.1:p.Gly125LysfsTer7
NM_006359.3:c.527_528insAAAAAGGA NP_006350.1:p.Gly177LysfsTer7
NM_001042537.2:c.623_624insAAAAAGGA NP_001036002.1:p.Gly209LysfsTer7
NM_001379110.1:c.467_468insAAAAAGGA MANE Select NP_001366039.1:p.Gly157LysfsTer7
NM_001400909.1:c.467_468insAAAAAGGA NP_001387838.1:p.Gly157LysfsTer7
NM_001400910.1:c.467_468insAAAAAGGA NP_001387839.1:p.Gly157LysfsTer7
NM_001400911.1:c.467_468insAAAAAGGA NP_001387840.1:p.Gly157LysfsTer7
NM_001400912.1:c.467_468insAAAAAGGA NP_001387841.1:p.Gly157LysfsTer7
NM_001400913.1:c.371_372insAAAAAGGA NP_001387842.1:p.Gly125LysfsTer7