Canonical Allele Identifier: CA1054439508

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1934011259
• gnomAD v3: 3-143707371-C-CACAG
• gnomAD v4: 3-143707371-C-CACAG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707374_143707375insGACA , CM000665.2:g.143707374_143707375insGACA	GRCh38
NC_000003.11:g.143426216_143426217insGACA , CM000665.1:g.143426216_143426217insGACA	GRCh37
NC_000003.10:g.144908906_144908907insGACA	NCBI36
NG_017077.1:g.146160_146161insCTGT
NG_017077.2:g.146160_146161insCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-14065_534-14064insCTGT MANE Select	ENSP00000320246.6:n.534-14065_534-14064insCTGT
ENST00000316549.10:c.534-14065_534-14064insCTGT	ENSP00000320246.6:n.534-14065_534-14064insCTGT
ENST00000474727.2:c.*145-14065_*145-14064insCTGT	ENSP00000419090.2:n.*145-14065_*145-14064insCTGT
NM_173653.3:c.534-14065_534-14064insCTGT	NP_775924.1:n.534-14065_534-14064insCTGT
XM_011512704.1:c.534-14065_534-14064insCTGT	XP_011511006.1:n.534-14065_534-14064insCTGT
XM_011512704.3:c.534-14065_534-14064insCTGT	XP_011511006.1:n.534-14065_534-14064insCTGT
XM_017006202.2:c.534-14065_534-14064insCTGT	XP_016861691.1:n.534-14065_534-14064insCTGT
XM_017006203.1:c.183-14065_183-14064insCTGT	XP_016861692.1:n.183-14065_183-14064insCTGT
NM_173653.4:c.534-14065_534-14064insCTGT MANE Select	NP_775924.1:n.534-14065_534-14064insCTGT