Canonical Allele Identifier: CA2460185426
Gene: SLC9A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.135985606G= , CM000685.2:g.135985606G= GRCh38
NC_000023.10:g.135067765G= , CM000685.1:g.135067765G= GRCh37
NC_000023.9:g.134895431G= NCBI36
NG_017160.1:g.5180G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370695.8:c.104G= ENSP00000359729.4:p.Gly35=
ENST00000370701.6:c.-53G= ENSP00000359735.1:n.-53G=
ENST00000630721.3:c.-53G= MANE Select ENSP00000487486.2:n.-53G=
ENST00000636092.1:c.-53G= ENSP00000490406.1:n.-53G=
ENST00000636347.1:c.-35-18G= ENSP00000490648.1:n.-35-18G=
ENST00000637195.1:c.-35-18G= ENSP00000490330.1:n.-35-18G=
ENST00000637234.1:c.-53G= ENSP00000490527.1:n.-53G=
ENST00000637581.1:c.-53G= ENSP00000490731.1:n.-53G=
ENST00000678163.1:c.104G= ENSP00000502845.1:p.Gly35=
ENST00000370695.6:c.104G= ENSP00000359729.4:p.Gly35=
ENST00000370698.7:c.104G= ENSP00000359732.3:p.Gly35=
ENST00000370701.5:c.-53G= ENSP00000359735.1:n.-53G=
ENST00000627534.2:c.-53G= ENSP00000486743.1:n.-53G=
NM_001042537.1:c.104G= NP_001036002.1:p.Gly35=
NM_001177651.1:c.-53G= NP_001171122.1:n.-53G=
NM_006359.2:c.104G= NP_006350.1:p.Gly35=
XM_006724726.2:c.-53G= XP_006724789.1:n.-53G=
XM_011531243.1:c.-53G= XP_011529545.1:n.-53G=
NM_001330652.1:c.-53G= NP_001317581.1:n.-53G=
XM_006724726.3:c.-53G= XP_006724789.1:n.-53G=
XM_017029223.2:c.-53G= XP_016884712.1:n.-53G=
XM_017029224.1:c.-53G= XP_016884713.1:n.-53G=
XM_017029225.1:c.-53G= XP_016884714.1:n.-53G=
NM_001177651.2:c.-53G= NP_001171122.1:n.-53G=
NM_001330652.2:c.-53G= NP_001317581.1:n.-53G=
NM_006359.3:c.104G= NP_006350.1:p.Gly35=
NM_001042537.2:c.104G= NP_001036002.1:p.Gly35=
NM_001379110.1:c.-53G= MANE Select NP_001366039.1:n.-53G=
NM_001400909.1:c.-35-18G= NP_001387838.1:n.-35-18G=
NM_001400910.1:c.-53G= NP_001387839.1:n.-53G=
NM_001400911.1:c.-53G= NP_001387840.1:n.-53G=
NM_001400912.1:c.-53G= NP_001387841.1:n.-53G=
NM_001400913.1:c.-53G= NP_001387842.1:n.-53G=