Canonical Allele Identifier: CA900031106

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1390162859
• gnomAD v3: 3-143705841-CT-C
• gnomAD v4: 3-143705841-CT-C
• MyVariant Identifiers: chr3:g.143424684del (hg19) ; chr3:g.143705842del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143705844del , CM000665.2:g.143705844del	GRCh38
NC_000003.11:g.143424686del , CM000665.1:g.143424686del	GRCh37
NC_000003.10:g.144907376del	NCBI36
NG_017077.1:g.147690del
NG_017077.2:g.147690del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-12535del MANE Select	ENSP00000320246.6:n.534-12535del
ENST00000316549.10:c.534-12535del	ENSP00000320246.6:n.534-12535del
ENST00000474727.2:c.*145-12535del	ENSP00000419090.2:n.*145-12535del
NM_173653.3:c.534-12535del	NP_775924.1:n.534-12535del
XM_011512704.1:c.534-12535del	XP_011511006.1:n.534-12535del
XM_011512704.3:c.534-12535del	XP_011511006.1:n.534-12535del
XM_017006202.2:c.534-12535del	XP_016861691.1:n.534-12535del
XM_017006203.1:c.183-12535del	XP_016861692.1:n.183-12535del
NM_173653.4:c.534-12535del MANE Select	NP_775924.1:n.534-12535del