Canonical Allele Identifier: CA1407571682

Gene: SLC9A9

Linked Data

• dbSNP Id: rs2008030223

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143785791_143785795dup , CM000665.2:g.143785791_143785795dup	GRCh38
NC_000003.11:g.143504633_143504637dup , CM000665.1:g.143504633_143504637dup	GRCh37
NC_000003.10:g.144987323_144987327dup	NCBI36
NG_017077.1:g.67737_67741dup
NG_017077.2:g.67737_67741dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.533+9206_533+9210dup MANE Select	ENSP00000320246.6:n.533+9206_533+9210dup
ENST00000316549.10:c.533+9206_533+9210dup	ENSP00000320246.6:n.533+9206_533+9210dup
ENST00000474727.2:c.*144+9206_*144+9210dup	ENSP00000419090.2:n.*144+9206_*144+9210du...
NM_173653.3:c.533+9206_533+9210dup	NP_775924.1:n.533+9206_533+9210dup
XM_011512704.1:c.533+9206_533+9210dup	XP_011511006.1:n.533+9206_533+9210dup
XM_011512704.3:c.533+9206_533+9210dup	XP_011511006.1:n.533+9206_533+9210dup
XM_017006202.2:c.533+9206_533+9210dup	XP_016861691.1:n.533+9206_533+9210dup
XM_017006203.1:c.182+9206_182+9210dup	XP_016861692.1:n.182+9206_182+9210dup
NM_173653.4:c.533+9206_533+9210dup MANE Select	NP_775924.1:n.533+9206_533+9210dup