Canonical Allele Identifier: CA1054438756

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1933955927
• gnomAD v3: 3-143705858-A-AGAAT
• gnomAD v4: 3-143705858-A-AGAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143705860_143705863dup , CM000665.2:g.143705860_143705863dup	GRCh38
NC_000003.11:g.143424702_143424705dup , CM000665.1:g.143424702_143424705dup	GRCh37
NC_000003.10:g.144907392_144907395dup	NCBI36
NG_017077.1:g.147670_147673dup
NG_017077.2:g.147670_147673dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-12555_534-12552dup MANE Select	ENSP00000320246.6:n.534-12555_534-12552dup
ENST00000316549.10:c.534-12555_534-12552dup	ENSP00000320246.6:n.534-12555_534-12552dup
ENST00000474727.2:c.*145-12555_*145-12552dup	ENSP00000419090.2:n.*145-12555_*145-12552dup
NM_173653.3:c.534-12555_534-12552dup	NP_775924.1:n.534-12555_534-12552dup
XM_011512704.1:c.534-12555_534-12552dup	XP_011511006.1:n.534-12555_534-12552dup
XM_011512704.3:c.534-12555_534-12552dup	XP_011511006.1:n.534-12555_534-12552dup
XM_017006202.2:c.534-12555_534-12552dup	XP_016861691.1:n.534-12555_534-12552dup
XM_017006203.1:c.183-12555_183-12552dup	XP_016861692.1:n.183-12555_183-12552dup
NM_173653.4:c.534-12555_534-12552dup MANE Select	NP_775924.1:n.534-12555_534-12552dup