Canonical Allele Identifier: CA546822744

Gene: SLC9A9

Linked Data

• dbSNP Id: rs757480379
• gnomAD v2: 3-143426244-C-CACACACA
• gnomAD v3: 3-143707402-C-CACACACA
• gnomAD v4: 3-143707402-C-CACACACA
• MyVariant Identifiers: chr3:g.143426244_143426245insACACACA (hg19) ; chr3:g.143707402_143707403insACACACA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707402_143707403insACACACA , CM000665.2:g.143707402_143707403insACACACA	GRCh38
NC_000003.11:g.143426244_143426245insACACACA , CM000665.1:g.143426244_143426245insACACACA	GRCh37
NC_000003.10:g.144908934_144908935insACACACA	NCBI36
NG_017077.1:g.146129_146130insTGTGTGT
NG_017077.2:g.146129_146130insTGTGTGT

Transcript Alleles

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