Canonical Allele Identifier: CA644596946

Gene: SLC9A6

Linked Data

• dbSNP Id: rs1303145725
• gnomAD v2: X-135067537-AGCG-A
• gnomAD v3: X-135985378-AGCG-A
• gnomAD v4: X-135985378-AGCG-A
• MyVariant Identifiers: chrX:g.135067538_135067540del (hg19) ; chrX:g.135985379_135985381del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.135985391_135985393del , CM000685.2:g.135985391_135985393del	GRCh38
NC_000023.10:g.135067550_135067552del , CM000685.1:g.135067550_135067552del	GRCh37
NC_000023.9:g.134895216_134895218del	NCBI36
NG_017160.1:g.4965_4967del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370701.6:c.-143_-141del	ENSP00000359735.1:n.-143_-141del
ENST00000636092.1:c.-56-212_-56-210del	ENSP00000490406.1:n.-56-212_-56-210del
ENST00000636347.1:c.-35-233_-35-231del	ENSP00000490648.1:n.-35-233_-35-231del
ENST00000637195.1:c.-35-233_-35-231del	ENSP00000490330.1:n.-35-233_-35-231del
ENST00000637234.1:c.-56-212_-56-210del	ENSP00000490527.1:n.-56-212_-56-210del
ENST00000637581.1:c.-56-212_-56-210del	ENSP00000490731.1:n.-56-212_-56-210del
XM_006724726.3:c.-138_-136del	XP_006724789.1:n.-138_-136del
XM_017029223.2:c.-56-212_-56-210del	XP_016884712.1:n.-56-212_-56-210del
XM_017029224.1:c.-56-212_-56-210del	XP_016884713.1:n.-56-212_-56-210del
NM_001400909.1:c.-35-233_-35-231del	NP_001387838.1:n.-35-233_-35-231del
NM_001400910.1:c.-56-212_-56-210del	NP_001387839.1:n.-56-212_-56-210del
NM_001400911.1:c.-56-212_-56-210del	NP_001387840.1:n.-56-212_-56-210del