Canonical Allele Identifier: CA2460185368
Gene: SLC9A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.135985492_135985493delinsCG , CM000685.2:g.135985492_135985493delinsCG GRCh38
NC_000023.10:g.135067651_135067652delinsCG , CM000685.1:g.135067651_135067652delinsCG GRCh37
NC_000023.9:g.134895317_134895318delinsCG NCBI36
NG_017160.1:g.5066_5067delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000370695.8:c.-11_-10delinsCG ENSP00000359729.4:n.-11_-10delinsCG
ENST00000370701.6:c.-57+15_-57+16delinsCG ENSP00000359735.1:n.-57+15_-57+16delinsCG
ENST00000630721.3:c.-57+15_-57+16delinsCG MANE Select ENSP00000487486.2:n.-57+15_-57+16delinsCG
ENST00000636092.1:c.-56-111_-56-110delinsCG ENSP00000490406.1:n.-56-111_-56-110delinsCG
ENST00000636347.1:c.-35-132_-35-131delinsCG ENSP00000490648.1:n.-35-132_-35-131delinsCG
ENST00000637195.1:c.-35-132_-35-131delinsCG ENSP00000490330.1:n.-35-132_-35-131delinsCG
ENST00000637234.1:c.-56-111_-56-110delinsCG ENSP00000490527.1:n.-56-111_-56-110delinsCG
ENST00000637581.1:c.-56-111_-56-110delinsCG ENSP00000490731.1:n.-56-111_-56-110delinsCG
ENST00000678163.1:c.-11_-10delinsCG ENSP00000502845.1:n.-11_-10delinsCG
ENST00000370695.6:c.-11_-10delinsCG ENSP00000359729.4:n.-11_-10delinsCG
ENST00000370698.7:c.-11_-10delinsCG ENSP00000359732.3:n.-11_-10delinsCG
ENST00000370701.5:c.-57+15_-57+16delinsCG ENSP00000359735.1:n.-57+15_-57+16delinsCG
ENST00000627534.2:c.-57+20_-57+21delinsCG ENSP00000486743.1:n.-57+20_-57+21delinsCG
NM_001042537.1:c.-11_-10delinsCG NP_001036002.1:n.-11_-10delinsCG
NM_001177651.1:c.-57+15_-57+16delinsCG NP_001171122.1:n.-57+15_-57+16delinsCG
NM_006359.2:c.-11_-10delinsCG NP_006350.1:n.-11_-10delinsCG
XM_006724726.2:c.-57+20_-57+21delinsCG XP_006724789.1:n.-57+20_-57+21delinsCG
XM_011531243.1:c.-57+20_-57+21delinsCG XP_011529545.1:n.-57+20_-57+21delinsCG
NM_001330652.1:c.-57+20_-57+21delinsCG NP_001317581.1:n.-57+20_-57+21delinsCG
XM_006724726.3:c.-57+20_-57+21delinsCG XP_006724789.1:n.-57+20_-57+21delinsCG
XM_017029223.2:c.-56-111_-56-110delinsCG XP_016884712.1:n.-56-111_-56-110delinsCG
XM_017029224.1:c.-56-111_-56-110delinsCG XP_016884713.1:n.-56-111_-56-110delinsCG
XM_017029225.1:c.-57+15_-57+16delinsCG XP_016884714.1:n.-57+15_-57+16delinsCG
NM_001177651.2:c.-57+15_-57+16delinsCG NP_001171122.1:n.-57+15_-57+16delinsCG
NM_001330652.2:c.-57+20_-57+21delinsCG NP_001317581.1:n.-57+20_-57+21delinsCG
NM_006359.3:c.-11_-10delinsCG NP_006350.1:n.-11_-10delinsCG
NM_001042537.2:c.-11_-10delinsCG NP_001036002.1:n.-11_-10delinsCG
NM_001379110.1:c.-57+15_-57+16delinsCG MANE Select NP_001366039.1:n.-57+15_-57+16delinsCG
NM_001400909.1:c.-35-132_-35-131delinsCG NP_001387838.1:n.-35-132_-35-131delinsCG
NM_001400910.1:c.-56-111_-56-110delinsCG NP_001387839.1:n.-56-111_-56-110delinsCG
NM_001400911.1:c.-56-111_-56-110delinsCG NP_001387840.1:n.-56-111_-56-110delinsCG
NM_001400912.1:c.-57+20_-57+21delinsCG NP_001387841.1:n.-57+20_-57+21delinsCG
NM_001400913.1:c.-57+15_-57+16delinsCG NP_001387842.1:n.-57+15_-57+16delinsCG