Canonical Allele Identifier: CA518490255

Gene: SLC9A6

Linked Data

• dbSNP Id: rs782008453
• MyVariant Identifiers: chrX:g.135067469_135067470del (hg19) ; chrX:g.135985310_135985311del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.135985313_135985314del , CM000685.2:g.135985313_135985314del	GRCh38
NC_000023.10:g.135067472_135067473del , CM000685.1:g.135067472_135067473del	GRCh37
NC_000023.9:g.134895138_134895139del	NCBI36
NG_017160.1:g.4887_4888del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370701.6:c.-221_-220del	ENSP00000359735.1:n.-221_-220del
ENST00000636092.1:c.-56-290_-56-289del	ENSP00000490406.1:n.-56-290_-56-289del
ENST00000636347.1:c.-35-311_-35-310del	ENSP00000490648.1:n.-35-311_-35-310del
ENST00000637195.1:c.-35-311_-35-310del	ENSP00000490330.1:n.-35-311_-35-310del
ENST00000637234.1:c.-56-290_-56-289del	ENSP00000490527.1:n.-56-290_-56-289del
ENST00000637581.1:c.-56-290_-56-289del	ENSP00000490731.1:n.-56-290_-56-289del
XM_006724726.3:c.-216_-215del	XP_006724789.1:n.-216_-215del
XM_017029223.2:c.-56-290_-56-289del	XP_016884712.1:n.-56-290_-56-289del
XM_017029224.1:c.-56-290_-56-289del	XP_016884713.1:n.-56-290_-56-289del
NM_001400909.1:c.-35-311_-35-310del	NP_001387838.1:n.-35-311_-35-310del
NM_001400910.1:c.-56-290_-56-289del	NP_001387839.1:n.-56-290_-56-289del
NM_001400911.1:c.-56-290_-56-289del	NP_001387840.1:n.-56-290_-56-289del