Canonical Allele Identifier: CA2460185428
Gene: SLC9A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.135985612T= , CM000685.2:g.135985612T= GRCh38
NC_000023.10:g.135067771T= , CM000685.1:g.135067771T= GRCh37
NC_000023.9:g.134895437T= NCBI36
NG_017160.1:g.5186T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370695.8:c.110T= ENSP00000359729.4:p.Phe37=
ENST00000370701.6:c.-47T= ENSP00000359735.1:n.-47T=
ENST00000630721.3:c.-47T= MANE Select ENSP00000487486.2:n.-47T=
ENST00000636092.1:c.-47T= ENSP00000490406.1:n.-47T=
ENST00000636347.1:c.-35-12T= ENSP00000490648.1:n.-35-12T=
ENST00000637195.1:c.-35-12T= ENSP00000490330.1:n.-35-12T=
ENST00000637234.1:c.-47T= ENSP00000490527.1:n.-47T=
ENST00000637581.1:c.-47T= ENSP00000490731.1:n.-47T=
ENST00000678163.1:c.110T= ENSP00000502845.1:p.Phe37=
ENST00000370695.6:c.110T= ENSP00000359729.4:p.Phe37=
ENST00000370698.7:c.110T= ENSP00000359732.3:p.Phe37=
ENST00000370701.5:c.-47T= ENSP00000359735.1:n.-47T=
ENST00000627534.2:c.-47T= ENSP00000486743.1:n.-47T=
NM_001042537.1:c.110T= NP_001036002.1:p.Phe37=
NM_001177651.1:c.-47T= NP_001171122.1:n.-47T=
NM_006359.2:c.110T= NP_006350.1:p.Phe37=
XM_006724726.2:c.-47T= XP_006724789.1:n.-47T=
XM_011531243.1:c.-47T= XP_011529545.1:n.-47T=
NM_001330652.1:c.-47T= NP_001317581.1:n.-47T=
XM_006724726.3:c.-47T= XP_006724789.1:n.-47T=
XM_017029223.2:c.-47T= XP_016884712.1:n.-47T=
XM_017029224.1:c.-47T= XP_016884713.1:n.-47T=
XM_017029225.1:c.-47T= XP_016884714.1:n.-47T=
NM_001177651.2:c.-47T= NP_001171122.1:n.-47T=
NM_001330652.2:c.-47T= NP_001317581.1:n.-47T=
NM_006359.3:c.110T= NP_006350.1:p.Phe37=
NM_001042537.2:c.110T= NP_001036002.1:p.Phe37=
NM_001379110.1:c.-47T= MANE Select NP_001366039.1:n.-47T=
NM_001400909.1:c.-35-12T= NP_001387838.1:n.-35-12T=
NM_001400910.1:c.-47T= NP_001387839.1:n.-47T=
NM_001400911.1:c.-47T= NP_001387840.1:n.-47T=
NM_001400912.1:c.-47T= NP_001387841.1:n.-47T=
NM_001400913.1:c.-47T= NP_001387842.1:n.-47T=