Canonical Allele Identifier: CA1407571672

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1185064103

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143785781del , CM000665.2:g.143785781del	GRCh38
NC_000003.11:g.143504623del , CM000665.1:g.143504623del	GRCh37
NC_000003.10:g.144987313del	NCBI36
NG_017077.1:g.67757del
NG_017077.2:g.67757del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.533+9226del MANE Select	ENSP00000320246.6:n.533+9226del
ENST00000316549.10:c.533+9226del	ENSP00000320246.6:n.533+9226del
ENST00000474727.2:c.*144+9226del	ENSP00000419090.2:n.*144+9226del
NM_173653.3:c.533+9226del	NP_775924.1:n.533+9226del
XM_011512704.1:c.533+9226del	XP_011511006.1:n.533+9226del
XM_011512704.3:c.533+9226del	XP_011511006.1:n.533+9226del
XM_017006202.2:c.533+9226del	XP_016861691.1:n.533+9226del
XM_017006203.1:c.182+9226del	XP_016861692.1:n.182+9226del
NM_173653.4:c.533+9226del MANE Select	NP_775924.1:n.533+9226del