Canonical Allele Identifier: CA1054439595

Gene: SLC9A9

Linked Data

• dbSNP Id: rs757480379
• gnomAD v3: 3-143707402-C-CACA
• gnomAD v4: 3-143707402-C-CACA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707402_143707403insACA , CM000665.2:g.143707402_143707403insACA	GRCh38
NC_000003.11:g.143426244_143426245insACA , CM000665.1:g.143426244_143426245insACA	GRCh37
NC_000003.10:g.144908934_144908935insACA	NCBI36
NG_017077.1:g.146129_146130insTGT
NG_017077.2:g.146129_146130insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-14096_534-14095insTGT MANE Select	ENSP00000320246.6:n.534-14096_534-14095insTGT
ENST00000316549.10:c.534-14096_534-14095insTGT	ENSP00000320246.6:n.534-14096_534-14095insTGT
ENST00000474727.2:c.*145-14096_*145-14095insTGT	ENSP00000419090.2:n.*145-14096_*145-14095insTGT
NM_173653.3:c.534-14096_534-14095insTGT	NP_775924.1:n.534-14096_534-14095insTGT
XM_011512704.1:c.534-14096_534-14095insTGT	XP_011511006.1:n.534-14096_534-14095insTGT
XM_011512704.3:c.534-14096_534-14095insTGT	XP_011511006.1:n.534-14096_534-14095insTGT
XM_017006202.2:c.534-14096_534-14095insTGT	XP_016861691.1:n.534-14096_534-14095insTGT
XM_017006203.1:c.183-14096_183-14095insTGT	XP_016861692.1:n.183-14096_183-14095insTGT
NM_173653.4:c.534-14096_534-14095insTGT MANE Select	NP_775924.1:n.534-14096_534-14095insTGT