Canonical Allele Identifier: CA900065617

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1401327267
• gnomAD v3: 3-143785734-CTTGG-C
• gnomAD v4: 3-143785734-CTTGG-C
• MyVariant Identifiers: chr3:g.143504577_143504580del (hg19) ; chr3:g.143785735_143785738del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143785739_143785742del , CM000665.2:g.143785739_143785742del	GRCh38
NC_000003.11:g.143504581_143504584del , CM000665.1:g.143504581_143504584del	GRCh37
NC_000003.10:g.144987271_144987274del	NCBI36
NG_017077.1:g.67794_67797del
NG_017077.2:g.67794_67797del

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.533+9263_533+9266del MANE Select	ENSP00000320246.6:n.533+9263_533+9266del
ENST00000316549.10:c.533+9263_533+9266del	ENSP00000320246.6:n.533+9263_533+9266del
ENST00000474727.2:c.*144+9263_*144+9266del	ENSP00000419090.2:n.*144+9263_*144+9266de...
NM_173653.3:c.533+9263_533+9266del	NP_775924.1:n.533+9263_533+9266del
XM_011512704.1:c.533+9263_533+9266del	XP_011511006.1:n.533+9263_533+9266del
XM_011512704.3:c.533+9263_533+9266del	XP_011511006.1:n.533+9263_533+9266del
XM_017006202.2:c.533+9263_533+9266del	XP_016861691.1:n.533+9263_533+9266del
XM_017006203.1:c.182+9263_182+9266del	XP_016861692.1:n.182+9263_182+9266del
NM_173653.4:c.533+9263_533+9266del MANE Select	NP_775924.1:n.533+9263_533+9266del