Canonical Allele Identifier: CA871868065
Gene: SLC9A6 HGNC NCBI

Linked Data

dbSNP Id: rs1405557837
gnomAD v4: X-135985504-TGGCTC-T
MyVariant Identifiers: chrX:g.135985505_135985509del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.135985508_135985512del , CM000685.2:g.135985508_135985512del GRCh38
NC_000023.10:g.135067667_135067671del , CM000685.1:g.135067667_135067671del GRCh37
NC_000023.9:g.134895333_134895337del NCBI36
NG_017160.1:g.5082_5086del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370695.8:c.6_10del ENSP00000359729.4:p.Arg4LeufsTer?
ENST00000370701.6:c.-57+31_-57+35del ENSP00000359735.1:n.-57+31_-57+35del
ENST00000630721.3:c.-57+31_-57+35del MANE Select ENSP00000487486.2:n.-57+31_-57+35del
ENST00000636092.1:c.-56-95_-56-91del ENSP00000490406.1:n.-56-95_-56-91del
ENST00000636347.1:c.-35-116_-35-112del ENSP00000490648.1:n.-35-116_-35-112del
ENST00000637195.1:c.-35-116_-35-112del ENSP00000490330.1:n.-35-116_-35-112del
ENST00000637234.1:c.-56-95_-56-91del ENSP00000490527.1:n.-56-95_-56-91del
ENST00000637581.1:c.-56-95_-56-91del ENSP00000490731.1:n.-56-95_-56-91del
ENST00000678163.1:c.6_10del ENSP00000502845.1:p.Arg4LeufsTer?
ENST00000370695.6:c.6_10del ENSP00000359729.4:p.Arg4LeufsTer?
ENST00000370698.7:c.6_10del ENSP00000359732.3:p.Arg4LeufsTer?
ENST00000370701.5:c.-57+31_-57+35del ENSP00000359735.1:n.-57+31_-57+35del
ENST00000627534.2:c.-57+36_-57+40del ENSP00000486743.1:n.-57+36_-57+40del
NM_001042537.1:c.6_10del NP_001036002.1:p.Arg4LeufsTer?
NM_001177651.1:c.-57+31_-57+35del NP_001171122.1:n.-57+31_-57+35del
NM_006359.2:c.6_10del NP_006350.1:p.Arg4LeufsTer?
XM_006724726.2:c.-57+36_-57+40del XP_006724789.1:n.-57+36_-57+40del
XM_011531243.1:c.-57+36_-57+40del XP_011529545.1:n.-57+36_-57+40del
NM_001330652.1:c.-57+36_-57+40del NP_001317581.1:n.-57+36_-57+40del
XM_006724726.3:c.-57+36_-57+40del XP_006724789.1:n.-57+36_-57+40del
XM_017029223.2:c.-56-95_-56-91del XP_016884712.1:n.-56-95_-56-91del
XM_017029224.1:c.-56-95_-56-91del XP_016884713.1:n.-56-95_-56-91del
XM_017029225.1:c.-57+31_-57+35del XP_016884714.1:n.-57+31_-57+35del
NM_001177651.2:c.-57+31_-57+35del NP_001171122.1:n.-57+31_-57+35del
NM_001330652.2:c.-57+36_-57+40del NP_001317581.1:n.-57+36_-57+40del
NM_006359.3:c.6_10del NP_006350.1:p.Arg4LeufsTer?
NM_001042537.2:c.6_10del NP_001036002.1:p.Arg4LeufsTer?
NM_001379110.1:c.-57+31_-57+35del MANE Select NP_001366039.1:n.-57+31_-57+35del
NM_001400909.1:c.-35-116_-35-112del NP_001387838.1:n.-35-116_-35-112del
NM_001400910.1:c.-56-95_-56-91del NP_001387839.1:n.-56-95_-56-91del
NM_001400911.1:c.-56-95_-56-91del NP_001387840.1:n.-56-95_-56-91del
NM_001400912.1:c.-57+36_-57+40del NP_001387841.1:n.-57+36_-57+40del
NM_001400913.1:c.-57+31_-57+35del NP_001387842.1:n.-57+31_-57+35del
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