Canonical Allele Identifier: CA2823729192
Gene: SLC9A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.135998479_135998483del , CM000685.2:g.135998479_135998483del GRCh38
NC_000023.10:g.135080638_135080642del , CM000685.1:g.135080638_135080642del GRCh37
NC_000023.9:g.134908304_134908308del NCBI36
NG_017160.1:g.18053_18057del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370695.8:c.604-3_605del
ENST00000370701.6:c.448-3_449del
ENST00000630721.3:c.448-3_449del
ENST00000636092.1:c.448-3_449del
ENST00000636347.1:c.448-3_449del
ENST00000637195.1:c.352-3_353del
ENST00000637234.1:c.448-3_449del
ENST00000637581.1:c.448-3_449del
ENST00000643775.1:n.391-3_392del
ENST00000674809.1:c.391-3_392del
ENST00000675550.1:n.389-3_390del
ENST00000675856.1:n.391-3_392del
ENST00000676043.1:c.391-3_392del
ENST00000678163.1:c.604-3_605del
ENST00000370695.6:c.604-3_605del
ENST00000370698.7:c.508-3_509del
ENST00000370701.5:c.448-3_449del
ENST00000627534.2:c.448-3_449del
NM_001042537.1:c.604-3_605del
NM_001177651.1:c.448-3_449del
NM_006359.2:c.508-3_509del
XM_006724726.2:c.448-3_449del
XM_011531243.1:c.352-3_353del
NM_001330652.1:c.352-3_353del
XM_006724726.3:c.448-3_449del
XM_017029223.2:c.448-3_449del
XM_017029224.1:c.448-3_449del
XM_017029225.1:c.352-3_353del
NM_001177651.2:c.448-3_449del
NM_001330652.2:c.352-3_353del
NM_006359.3:c.508-3_509del
NM_001042537.2:c.604-3_605del
NM_001379110.1:c.448-3_449del
NM_001400909.1:c.448-3_449del
NM_001400910.1:c.448-3_449del
NM_001400911.1:c.448-3_449del
NM_001400912.1:c.448-3_449del
NM_001400913.1:c.352-3_353del