Canonical Allele Identifier: CA546822727

Gene: SLC9A9

Linked Data

• dbSNP Id: rs898307304
• gnomAD v2: 3-143426227-C-CACACAA
• gnomAD v3: 3-143707385-C-CACACAA
• gnomAD v4: 3-143707385-C-CACACAA
• MyVariant Identifiers: chr3:g.143426227_143426228insACACAA (hg19) ; chr3:g.143707385_143707386insACACAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707390_143707391insAACACA , CM000665.2:g.143707390_143707391insAACACA	GRCh38
NC_000003.11:g.143426232_143426233insAACACA , CM000665.1:g.143426232_143426233insAACACA	GRCh37
NC_000003.10:g.144908922_144908923insAACACA	NCBI36
NG_017077.1:g.146146_146147insTTGTGT
NG_017077.2:g.146146_146147insTTGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-14079_534-14078insTTGTGT MANE Select	ENSP00000320246.6:n.534-14079_534-14078insTTGTGT
ENST00000316549.10:c.534-14079_534-14078insTTGTGT	ENSP00000320246.6:n.534-14079_534-14078insTTGTGT
ENST00000474727.2:c.*145-14079_*145-14078insTTGTGT	ENSP00000419090.2:n.*145-14079_*145-14078insTTGTGT
NM_173653.3:c.534-14079_534-14078insTTGTGT	NP_775924.1:n.534-14079_534-14078insTTGTGT
XM_011512704.1:c.534-14079_534-14078insTTGTGT	XP_011511006.1:n.534-14079_534-14078insTTGTGT
XM_011512704.3:c.534-14079_534-14078insTTGTGT	XP_011511006.1:n.534-14079_534-14078insTTGTGT
XM_017006202.2:c.534-14079_534-14078insTTGTGT	XP_016861691.1:n.534-14079_534-14078insTTGTGT
XM_017006203.1:c.183-14079_183-14078insTTGTGT	XP_016861692.1:n.183-14079_183-14078insTTGTGT
NM_173653.4:c.534-14079_534-14078insTTGTGT MANE Select	NP_775924.1:n.534-14079_534-14078insTTGTGT