Canonical Allele Identifier: CA16621204
Gene: SLC9A6 HGNC NCBI

Linked Data

dbSNP Id: rs1064795183

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.135998483_135998484del , CM000685.2:g.135998483_135998484del GRCh38
NC_000023.10:g.135080642_135080643del , CM000685.1:g.135080642_135080643del GRCh37
NC_000023.9:g.134908308_134908309del NCBI36
NG_017160.1:g.18057_18058del

Transcript Alleles

HGVS Amino-acid change
ENST00000370695.8:c.605_606del
ENST00000370701.6:c.449_450del
ENST00000630721.3:c.449_450del
ENST00000636092.1:c.449_450del
ENST00000636347.1:c.449_450del
ENST00000637195.1:c.353_354del
ENST00000637234.1:c.449_450del
ENST00000637581.1:c.449_450del
ENST00000643775.1:n.392_393del
ENST00000674809.1:c.392_393del
ENST00000675550.1:n.390_391del
ENST00000675856.1:n.392_393del
ENST00000676043.1:c.392_393del
ENST00000678163.1:c.605_606del
ENST00000370695.6:c.605_606del
ENST00000370698.7:c.509_510del
ENST00000370701.5:c.449_450del
ENST00000627534.2:c.449_450del
NM_001042537.1:c.605_606del
NM_001177651.1:c.449_450del
NM_006359.2:c.509_510del
XM_006724726.2:c.449_450del
XM_011531243.1:c.353_354del
NM_001330652.1:c.353_354del
XM_006724726.3:c.449_450del
XM_017029223.2:c.449_450del
XM_017029224.1:c.449_450del
XM_017029225.1:c.353_354del
NM_001177651.2:c.449_450del
NM_001330652.2:c.353_354del
NM_006359.3:c.509_510del
NM_001042537.2:c.605_606del
NM_001379110.1:c.449_450del
NM_001400909.1:c.449_450del
NM_001400910.1:c.449_450del
NM_001400911.1:c.449_450del
NM_001400912.1:c.449_450del
NM_001400913.1:c.353_354del