Canonical Allele Identifier: CA899976666

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1394256752
• gnomAD v3: 3-143337577-G-GA
• gnomAD v4: 3-143337577-G-GA
• MyVariant Identifiers: chr3:g.143056419_143056420insA (hg19) ; chr3:g.143337577_143337578insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143337579dup , CM000665.2:g.143337579dup	GRCh38
NC_000003.11:g.143056421dup , CM000665.1:g.143056421dup	GRCh37
NC_000003.10:g.144539111dup	NCBI36
NG_017077.1:g.515954dup
NG_017077.2:g.515954dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1604+25906dup MANE Select	ENSP00000320246.6:n.1604+25906dup
ENST00000316549.10:c.1604+25906dup	ENSP00000320246.6:n.1604+25906dup
NM_173653.3:c.1604+25906dup	NP_775924.1:n.1604+25906dup
XM_011512703.1:c.956+25906dup	XP_011511005.1:n.956+25906dup
XM_011512703.3:c.956+25906dup	XP_011511005.1:n.956+25906dup
XM_017006202.2:c.1711+25799dup	XP_016861691.1:n.1711+25799dup
XM_017006203.1:c.1253+25906dup	XP_016861692.1:n.1253+25906dup
NM_173653.4:c.1604+25906dup MANE Select	NP_775924.1:n.1604+25906dup