Canonical Allele Identifier: CA2580101559
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1803005
ClinVar RCV Id: RCV002466304

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.135998473_135998493del , CM000685.2:g.135998473_135998493del GRCh38
NC_000023.10:g.135080632_135080652del , CM000685.1:g.135080632_135080652del GRCh37
NC_000023.9:g.134908298_134908318del NCBI36
NG_017160.1:g.18047_18067del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370695.8:c.604-9_615del
ENST00000370701.6:c.448-9_459del
ENST00000630721.3:c.448-9_459del
ENST00000636092.1:c.448-9_459del
ENST00000636347.1:c.448-9_459del
ENST00000637195.1:c.352-9_363del
ENST00000637234.1:c.448-9_459del
ENST00000637581.1:c.448-9_459del
ENST00000643775.1:n.391-9_402del
ENST00000674809.1:c.391-9_402del
ENST00000675550.1:n.389-9_400del
ENST00000675856.1:n.391-9_402del
ENST00000676043.1:c.391-9_402del
ENST00000678163.1:c.604-9_615del
ENST00000370695.6:c.604-9_615del
ENST00000370698.7:c.508-9_519del
ENST00000370701.5:c.448-9_459del
ENST00000627534.2:c.448-9_459del
NM_001042537.1:c.604-9_615del
NM_001177651.1:c.448-9_459del
NM_006359.2:c.508-9_519del
XM_006724726.2:c.448-9_459del
XM_011531243.1:c.352-9_363del
NM_001330652.1:c.352-9_363del
XM_006724726.3:c.448-9_459del
XM_017029223.2:c.448-9_459del
XM_017029224.1:c.448-9_459del
XM_017029225.1:c.352-9_363del
NM_001177651.2:c.448-9_459del
NM_001330652.2:c.352-9_363del
NM_006359.3:c.508-9_519del
NM_001042537.2:c.604-9_615del
NM_001379110.1:c.448-9_459del
NM_001400909.1:c.448-9_459del
NM_001400910.1:c.448-9_459del
NM_001400911.1:c.448-9_459del
NM_001400912.1:c.448-9_459del
NM_001400913.1:c.352-9_363del