Canonical Allele Identifier: CA414750021
Gene: SLC9A6 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135080706T>A (hg19) chrX:g.135998547T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.135998547T>A , CM000685.2:g.135998547T>A GRCh38
NC_000023.10:g.135080706T>A , CM000685.1:g.135080706T>A GRCh37
NC_000023.9:g.134908372T>A NCBI36
NG_017160.1:g.18121T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370695.8:c.669T>A ENSP00000359729.4:p.Cys223Ter
ENST00000370701.6:c.513T>A ENSP00000359735.1:p.Cys171Ter
ENST00000630721.3:c.513T>A MANE Select ENSP00000487486.2:p.Cys171Ter
ENST00000636092.1:c.513T>A ENSP00000490406.1:p.Cys171Ter
ENST00000636347.1:c.513T>A ENSP00000490648.1:p.Cys171Ter
ENST00000637195.1:c.417T>A ENSP00000490330.1:p.Cys139Ter
ENST00000637234.1:c.513T>A ENSP00000490527.1:p.Cys171Ter
ENST00000637581.1:c.513T>A ENSP00000490731.1:p.Cys171Ter
ENST00000643775.1:n.456T>A
ENST00000674809.1:c.456T>A ENSP00000502455.1:p.Cys152Ter
ENST00000675550.1:n.454T>A
ENST00000675856.1:n.456T>A
ENST00000676043.1:c.456T>A ENSP00000501920.1:p.Cys152Ter
ENST00000678163.1:c.669T>A ENSP00000502845.1:p.Cys223Ter
ENST00000370695.6:c.669T>A ENSP00000359729.4:p.Cys223Ter
ENST00000370698.7:c.573T>A ENSP00000359732.3:p.Cys191Ter
ENST00000370701.5:c.513T>A ENSP00000359735.1:p.Cys171Ter
ENST00000627534.2:c.513T>A ENSP00000486743.1:p.Cys171Ter
NM_001042537.1:c.669T>A NP_001036002.1:p.Cys223Ter
NM_001177651.1:c.513T>A NP_001171122.1:p.Cys171Ter
NM_006359.2:c.573T>A NP_006350.1:p.Cys191Ter
XM_006724726.2:c.513T>A XP_006724789.1:p.Cys171Ter
XM_011531243.1:c.417T>A XP_011529545.1:p.Cys139Ter
NM_001330652.1:c.417T>A NP_001317581.1:p.Cys139Ter
XM_006724726.3:c.513T>A XP_006724789.1:p.Cys171Ter
XM_017029223.2:c.513T>A XP_016884712.1:p.Cys171Ter
XM_017029224.1:c.513T>A XP_016884713.1:p.Cys171Ter
XM_017029225.1:c.417T>A XP_016884714.1:p.Cys139Ter
NM_001177651.2:c.513T>A NP_001171122.1:p.Cys171Ter
NM_001330652.2:c.417T>A NP_001317581.1:p.Cys139Ter
NM_006359.3:c.573T>A NP_006350.1:p.Cys191Ter
NM_001042537.2:c.669T>A NP_001036002.1:p.Cys223Ter
NM_001379110.1:c.513T>A MANE Select NP_001366039.1:p.Cys171Ter
NM_001400909.1:c.513T>A NP_001387838.1:p.Cys171Ter
NM_001400910.1:c.513T>A NP_001387839.1:p.Cys171Ter
NM_001400911.1:c.513T>A NP_001387840.1:p.Cys171Ter
NM_001400912.1:c.513T>A NP_001387841.1:p.Cys171Ter
NM_001400913.1:c.417T>A NP_001387842.1:p.Cys139Ter
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