Canonical Allele Identifier: CA1407571656

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143785738_143785739delinsGT , CM000665.2:g.143785738_143785739delinsGT	GRCh38
NC_000003.11:g.143504580_143504581delinsGT , CM000665.1:g.143504580_143504581delinsGT	GRCh37
NC_000003.10:g.144987270_144987271delinsGT	NCBI36
NG_017077.1:g.67793_67794delinsAC
NG_017077.2:g.67793_67794delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.533+9262_533+9263delinsAC MANE Select	ENSP00000320246.6:n.533+9262_533+9263deli...
ENST00000316549.10:c.533+9262_533+9263delinsAC	ENSP00000320246.6:n.533+9262_533+9263deli...
ENST00000474727.2:c.*144+9262_*144+9263delinsAC	ENSP00000419090.2:n.*144+9262_*144+9263de...
NM_173653.3:c.533+9262_533+9263delinsAC	NP_775924.1:n.533+9262_533+9263delinsAC
XM_011512704.1:c.533+9262_533+9263delinsAC	XP_011511006.1:n.533+9262_533+9263delinsA...
XM_011512704.3:c.533+9262_533+9263delinsAC	XP_011511006.1:n.533+9262_533+9263delinsA...
XM_017006202.2:c.533+9262_533+9263delinsAC	XP_016861691.1:n.533+9262_533+9263delinsA...
XM_017006203.1:c.182+9262_182+9263delinsAC	XP_016861692.1:n.182+9262_182+9263delinsA...
NM_173653.4:c.533+9262_533+9263delinsAC MANE Select	NP_775924.1:n.533+9262_533+9263delinsAC