Canonical Allele Identifier: CA1054427422

Gene: SLC9A9

Linked Data

• gnomAD v3: 3-143785721-ACAT-A
• gnomAD v4: 3-143785721-ACAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143785722_143785724del , CM000665.2:g.143785722_143785724del	GRCh38
NC_000003.11:g.143504564_143504566del , CM000665.1:g.143504564_143504566del	GRCh37
NC_000003.10:g.144987254_144987256del	NCBI36
NG_017077.1:g.67808_67810del
NG_017077.2:g.67808_67810del

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.533+9277_533+9279del MANE Select	ENSP00000320246.6:n.533+9277_533+9279del
ENST00000316549.10:c.533+9277_533+9279del	ENSP00000320246.6:n.533+9277_533+9279del
ENST00000474727.2:c.*144+9277_*144+9279del	ENSP00000419090.2:n.*144+9277_*144+9279de...
NM_173653.3:c.533+9277_533+9279del	NP_775924.1:n.533+9277_533+9279del
XM_011512704.1:c.533+9277_533+9279del	XP_011511006.1:n.533+9277_533+9279del
XM_011512704.3:c.533+9277_533+9279del	XP_011511006.1:n.533+9277_533+9279del
XM_017006202.2:c.533+9277_533+9279del	XP_016861691.1:n.533+9277_533+9279del
XM_017006203.1:c.182+9277_182+9279del	XP_016861692.1:n.182+9277_182+9279del
NM_173653.4:c.533+9277_533+9279del MANE Select	NP_775924.1:n.533+9277_533+9279del