Canonical Allele Identifier: CA2704323429

Gene: SLC9A9

Linked Data

• dbSNP Id: rs2108793753

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707388_143707389insTGTAGACACACACACA , CM000665.2:g.143707388_143707389insTGTAGACACACACACA	GRCh38
NC_000003.11:g.143426230_143426231insTGTAGACACACACACA , CM000665.1:g.143426230_143426231insTGTAGACACACACACA	GRCh37
NC_000003.10:g.144908920_144908921insTGTAGACACACACACA	NCBI36
NG_017077.1:g.146154_146155insCTACATGTGTGTGTGT
NG_017077.2:g.146154_146155insCTACATGTGTGTGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-14071_534-14070insCTACATGTGTGTGTGT MANE Select	ENSP00000320246.6:n.534-14071_534-14070insCTACATGTGTGTGTGT
ENST00000316549.10:c.534-14071_534-14070insCTACATGTGTGTGTGT	ENSP00000320246.6:n.534-14071_534-14070insCTACATGTGTGTGTGT
ENST00000474727.2:c.*145-14071_*145-14070insCTACATGTGTGTGTGT	ENSP00000419090.2:n.*145-14071_*145-14070insCTACATGTGTGTGTGT
NM_173653.3:c.534-14071_534-14070insCTACATGTGTGTGTGT	NP_775924.1:n.534-14071_534-14070insCTACATGTGTGTGTGT
XM_011512704.1:c.534-14071_534-14070insCTACATGTGTGTGTGT	XP_011511006.1:n.534-14071_534-14070insCTACATGTGTGTGTGT
XM_011512704.3:c.534-14071_534-14070insCTACATGTGTGTGTGT	XP_011511006.1:n.534-14071_534-14070insCTACATGTGTGTGTGT
XM_017006202.2:c.534-14071_534-14070insCTACATGTGTGTGTGT	XP_016861691.1:n.534-14071_534-14070insCTACATGTGTGTGTGT
XM_017006203.1:c.183-14071_183-14070insCTACATGTGTGTGTGT	XP_016861692.1:n.183-14071_183-14070insCTACATGTGTGTGTGT
NM_173653.4:c.534-14071_534-14070insCTACATGTGTGTGTGT MANE Select	NP_775924.1:n.534-14071_534-14070insCTACATGTGTGTGTGT