Canonical Allele Identifier: CA1407571619

Gene: SLC9A9

Linked Data

• dbSNP Id: rs2008025996

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143785677_143785680del , CM000665.2:g.143785677_143785680del	GRCh38
NC_000003.11:g.143504519_143504522del , CM000665.1:g.143504519_143504522del	GRCh37
NC_000003.10:g.144987209_144987212del	NCBI36
NG_017077.1:g.67854_67857del
NG_017077.2:g.67854_67857del

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.533+9323_533+9326del MANE Select	ENSP00000320246.6:n.533+9323_533+9326del
ENST00000316549.10:c.533+9323_533+9326del	ENSP00000320246.6:n.533+9323_533+9326del
ENST00000474727.2:c.*144+9323_*144+9326del	ENSP00000419090.2:n.*144+9323_*144+9326del
NM_173653.3:c.533+9323_533+9326del	NP_775924.1:n.533+9323_533+9326del
XM_011512704.1:c.533+9323_533+9326del	XP_011511006.1:n.533+9323_533+9326del
XM_011512704.3:c.533+9323_533+9326del	XP_011511006.1:n.533+9323_533+9326del
XM_017006202.2:c.533+9323_533+9326del	XP_016861691.1:n.533+9323_533+9326del
XM_017006203.1:c.182+9323_182+9326del	XP_016861692.1:n.182+9323_182+9326del
NM_173653.4:c.533+9323_533+9326del MANE Select	NP_775924.1:n.533+9323_533+9326del