Canonical Allele Identifier: CA2460189917
Gene: SLC9A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.135998476_135998477delinsTG , CM000685.2:g.135998476_135998477delinsTG GRCh38
NC_000023.10:g.135080635_135080636delinsTG , CM000685.1:g.135080635_135080636delinsTG GRCh37
NC_000023.9:g.134908301_134908302delinsTG NCBI36
NG_017160.1:g.18050_18051delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000370695.8:c.604-6_604-5delinsTG ENSP00000359729.4:n.604-6_604-5delinsTG
ENST00000370701.6:c.448-6_448-5delinsTG ENSP00000359735.1:n.448-6_448-5delinsTG
ENST00000630721.3:c.448-6_448-5delinsTG MANE Select ENSP00000487486.2:n.448-6_448-5delinsTG
ENST00000636092.1:c.448-6_448-5delinsTG ENSP00000490406.1:n.448-6_448-5delinsTG
ENST00000636347.1:c.448-6_448-5delinsTG ENSP00000490648.1:n.448-6_448-5delinsTG
ENST00000637195.1:c.352-6_352-5delinsTG ENSP00000490330.1:n.352-6_352-5delinsTG
ENST00000637234.1:c.448-6_448-5delinsTG ENSP00000490527.1:n.448-6_448-5delinsTG
ENST00000637581.1:c.448-6_448-5delinsTG ENSP00000490731.1:n.448-6_448-5delinsTG
ENST00000643775.1:n.391-6_391-5delinsTG
ENST00000674809.1:c.391-6_391-5delinsTG ENSP00000502455.1:n.391-6_391-5delinsTG
ENST00000675550.1:n.389-6_389-5delinsTG
ENST00000675856.1:n.391-6_391-5delinsTG
ENST00000676043.1:c.391-6_391-5delinsTG ENSP00000501920.1:n.391-6_391-5delinsTG
ENST00000678163.1:c.604-6_604-5delinsTG ENSP00000502845.1:n.604-6_604-5delinsTG
ENST00000370695.6:c.604-6_604-5delinsTG ENSP00000359729.4:n.604-6_604-5delinsTG
ENST00000370698.7:c.508-6_508-5delinsTG ENSP00000359732.3:n.508-6_508-5delinsTG
ENST00000370701.5:c.448-6_448-5delinsTG ENSP00000359735.1:n.448-6_448-5delinsTG
ENST00000627534.2:c.448-6_448-5delinsTG ENSP00000486743.1:n.448-6_448-5delinsTG
NM_001042537.1:c.604-6_604-5delinsTG NP_001036002.1:n.604-6_604-5delinsTG
NM_001177651.1:c.448-6_448-5delinsTG NP_001171122.1:n.448-6_448-5delinsTG
NM_006359.2:c.508-6_508-5delinsTG NP_006350.1:n.508-6_508-5delinsTG
XM_006724726.2:c.448-6_448-5delinsTG XP_006724789.1:n.448-6_448-5delinsTG
XM_011531243.1:c.352-6_352-5delinsTG XP_011529545.1:n.352-6_352-5delinsTG
NM_001330652.1:c.352-6_352-5delinsTG NP_001317581.1:n.352-6_352-5delinsTG
XM_006724726.3:c.448-6_448-5delinsTG XP_006724789.1:n.448-6_448-5delinsTG
XM_017029223.2:c.448-6_448-5delinsTG XP_016884712.1:n.448-6_448-5delinsTG
XM_017029224.1:c.448-6_448-5delinsTG XP_016884713.1:n.448-6_448-5delinsTG
XM_017029225.1:c.352-6_352-5delinsTG XP_016884714.1:n.352-6_352-5delinsTG
NM_001177651.2:c.448-6_448-5delinsTG NP_001171122.1:n.448-6_448-5delinsTG
NM_001330652.2:c.352-6_352-5delinsTG NP_001317581.1:n.352-6_352-5delinsTG
NM_006359.3:c.508-6_508-5delinsTG NP_006350.1:n.508-6_508-5delinsTG
NM_001042537.2:c.604-6_604-5delinsTG NP_001036002.1:n.604-6_604-5delinsTG
NM_001379110.1:c.448-6_448-5delinsTG MANE Select NP_001366039.1:n.448-6_448-5delinsTG
NM_001400909.1:c.448-6_448-5delinsTG NP_001387838.1:n.448-6_448-5delinsTG
NM_001400910.1:c.448-6_448-5delinsTG NP_001387839.1:n.448-6_448-5delinsTG
NM_001400911.1:c.448-6_448-5delinsTG NP_001387840.1:n.448-6_448-5delinsTG
NM_001400912.1:c.448-6_448-5delinsTG NP_001387841.1:n.448-6_448-5delinsTG
NM_001400913.1:c.352-6_352-5delinsTG NP_001387842.1:n.352-6_352-5delinsTG