Canonical Allele Identifier: CA10524756
Gene: SLC9A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136013395G>A , CM000685.2:g.136013395G>A GRCh38
NC_000023.10:g.135095554G>A , CM000685.1:g.135095554G>A GRCh37
NC_000023.9:g.134923220G>A NCBI36
NG_017160.1:g.32969G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001379110.1:c.1038G>A MANE Select NP_001366039.1:p.Thr346=
ENST00000630721.3:c.1038G>A MANE Select ENSP00000487486.2:p.Thr346=
NM_001042537.1:c.1194G>A NP_001036002.1:p.Thr398=
NM_001042537.2:c.1194G>A NP_001036002.1:p.Thr398=
NM_001177651.1:c.1038G>A NP_001171122.1:p.Thr346=
NM_001177651.2:c.1038G>A NP_001171122.1:p.Thr346=
NM_001330652.1:c.942G>A NP_001317581.1:p.Thr314=
NM_001330652.2:c.942G>A NP_001317581.1:p.Thr314=
NM_001400909.1:c.1038G>A NP_001387838.1:p.Thr346=
NM_001400910.1:c.1038G>A NP_001387839.1:p.Thr346=
NM_001400911.1:c.1038G>A NP_001387840.1:p.Thr346=
NM_001400912.1:c.1038G>A NP_001387841.1:p.Thr346=
NM_001400913.1:c.942G>A NP_001387842.1:p.Thr314=
NM_006359.2:c.1098G>A NP_006350.1:p.Thr366=
NM_006359.3:c.1098G>A NP_006350.1:p.Thr366=
ENST00000370695.6:c.1194G>A ENSP00000359729.4:p.Thr398=
ENST00000370695.8:c.1194G>A ENSP00000359729.4:p.Thr398=
ENST00000370698.7:c.1098G>A ENSP00000359732.3:p.Thr366=
ENST00000370701.5:c.1038G>A ENSP00000359735.1:p.Thr346=
ENST00000370701.6:c.1038G>A ENSP00000359735.1:p.Thr346=
ENST00000636092.1:c.1038G>A ENSP00000490406.1:p.Thr346=
ENST00000636347.1:c.1038G>A ENSP00000490648.1:p.Thr346=
ENST00000636798.1:n.473G>A
ENST00000637195.1:c.942G>A ENSP00000490330.1:p.Thr314=
ENST00000637234.1:c.1038G>A ENSP00000490527.1:p.Thr346=
ENST00000637581.1:c.1038G>A ENSP00000490731.1:p.Thr346=
ENST00000643775.1:n.981G>A
ENST00000675856.1:n.981G>A
ENST00000678163.1:c.1194G>A ENSP00000502845.1:p.Thr398=
XM_006724726.2:c.1038G>A XP_006724789.1:p.Thr346=
XM_006724726.3:c.1038G>A XP_006724789.1:p.Thr346=
XM_011531243.1:c.942G>A XP_011529545.1:p.Thr314=
XM_017029223.2:c.1038G>A XP_016884712.1:p.Thr346=
XM_017029224.1:c.1038G>A XP_016884713.1:p.Thr346=
XM_017029225.1:c.942G>A XP_016884714.1:p.Thr314=