Canonical Allele Identifier: CA1407536812

Gene: SLC9A9

Linked Data

• dbSNP Id: rs549058822

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707401_143707402insACCCCC , CM000665.2:g.143707401_143707402insACCCCC	GRCh38
NC_000003.11:g.143426243_143426244insACCCCC , CM000665.1:g.143426243_143426244insACCCCC	GRCh37
NC_000003.10:g.144908933_144908934insACCCCC	NCBI36
NG_017077.1:g.146131_146132insGGGGTG
NG_017077.2:g.146131_146132insGGGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-14094_534-14093insGGGGTG MANE Select	ENSP00000320246.6:n.534-14094_534-14093insGGGGTG
ENST00000316549.10:c.534-14094_534-14093insGGGGTG	ENSP00000320246.6:n.534-14094_534-14093insGGGGTG
ENST00000474727.2:c.*145-14094_*145-14093insGGGGTG	ENSP00000419090.2:n.*145-14094_*145-14093insGGGGTG
NM_173653.3:c.534-14094_534-14093insGGGGTG	NP_775924.1:n.534-14094_534-14093insGGGGTG
XM_011512704.1:c.534-14094_534-14093insGGGGTG	XP_011511006.1:n.534-14094_534-14093insGGGGTG
XM_011512704.3:c.534-14094_534-14093insGGGGTG	XP_011511006.1:n.534-14094_534-14093insGGGGTG
XM_017006202.2:c.534-14094_534-14093insGGGGTG	XP_016861691.1:n.534-14094_534-14093insGGGGTG
XM_017006203.1:c.183-14094_183-14093insGGGGTG	XP_016861692.1:n.183-14094_183-14093insGGGGTG
NM_173653.4:c.534-14094_534-14093insGGGGTG MANE Select	NP_775924.1:n.534-14094_534-14093insGGGGTG