Canonical Allele Identifier: CA2460185298

Gene: SLC9A6

Linked Data

• dbSNP Id: rs2089313939

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.135985397_135985398del , CM000685.2:g.135985397_135985398del	GRCh38
NC_000023.10:g.135067556_135067557del , CM000685.1:g.135067556_135067557del	GRCh37
NC_000023.9:g.134895222_134895223del	NCBI36
NG_017160.1:g.4971_4972del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370701.6:c.-137_-136del	ENSP00000359735.1:n.-137_-136del
ENST00000636092.1:c.-56-206_-56-205del	ENSP00000490406.1:n.-56-206_-56-205del
ENST00000636347.1:c.-35-227_-35-226del	ENSP00000490648.1:n.-35-227_-35-226del
ENST00000637195.1:c.-35-227_-35-226del	ENSP00000490330.1:n.-35-227_-35-226del
ENST00000637234.1:c.-56-206_-56-205del	ENSP00000490527.1:n.-56-206_-56-205del
ENST00000637581.1:c.-56-206_-56-205del	ENSP00000490731.1:n.-56-206_-56-205del
XM_006724726.3:c.-132_-131del	XP_006724789.1:n.-132_-131del
XM_017029223.2:c.-56-206_-56-205del	XP_016884712.1:n.-56-206_-56-205del
XM_017029224.1:c.-56-206_-56-205del	XP_016884713.1:n.-56-206_-56-205del
NM_001400909.1:c.-35-227_-35-226del	NP_001387838.1:n.-35-227_-35-226del
NM_001400910.1:c.-56-206_-56-205del	NP_001387839.1:n.-56-206_-56-205del
NM_001400911.1:c.-56-206_-56-205del	NP_001387840.1:n.-56-206_-56-205del