Canonical Allele Identifier: CA2605113791

Gene: SLC9A9

Linked Data

• gnomAD v3: 3-143785789-G-GTCTGAGGGTACTGAAGAATAAAGGTGAGCTGAGTAATTCTAAGACTTGA
• gnomAD v4: 3-143785789-G-GTCTGAGGGTACTGAAGAATAAAGGTGAGCTGAGTAATTCTAAGACTTGA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143785790_143785838dup , CM000665.2:g.143785790_143785838dup	GRCh38
NC_000003.11:g.143504632_143504680dup , CM000665.1:g.143504632_143504680dup	GRCh37
NC_000003.10:g.144987322_144987370dup	NCBI36
NG_017077.1:g.67694_67742dup
NG_017077.2:g.67694_67742dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.533+9163_533+9211dup MANE Select	ENSP00000320246.6:n.533+9163_533+9211dup
ENST00000316549.10:c.533+9163_533+9211dup	ENSP00000320246.6:n.533+9163_533+9211dup
ENST00000474727.2:c.*144+9163_*144+9211dup	ENSP00000419090.2:n.*144+9163_*144+9211dup
NM_173653.3:c.533+9163_533+9211dup	NP_775924.1:n.533+9163_533+9211dup
XM_011512704.1:c.533+9163_533+9211dup	XP_011511006.1:n.533+9163_533+9211dup
XM_011512704.3:c.533+9163_533+9211dup	XP_011511006.1:n.533+9163_533+9211dup
XM_017006202.2:c.533+9163_533+9211dup	XP_016861691.1:n.533+9163_533+9211dup
XM_017006203.1:c.182+9163_182+9211dup	XP_016861692.1:n.182+9163_182+9211dup
NM_173653.4:c.533+9163_533+9211dup MANE Select	NP_775924.1:n.533+9163_533+9211dup