Canonical Allele Identifier: CA85301688

Gene: SLC9A9

Linked Data

• dbSNP Id: rs552132760
• gnomAD v2: 3-143424745-GA-G
• gnomAD v3: 3-143705903-GA-G
• gnomAD v4: 3-143705903-GA-G
• MyVariant Identifiers: chr3:g.143424746del (hg19) ; chr3:g.143705904del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143705904del , CM000665.2:g.143705904del	GRCh38
NC_000003.11:g.143424746del , CM000665.1:g.143424746del	GRCh37
NC_000003.10:g.144907436del	NCBI36
NG_017077.1:g.147628del
NG_017077.2:g.147628del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-12597del MANE Select	ENSP00000320246.6:n.534-12597del
ENST00000316549.10:c.534-12597del	ENSP00000320246.6:n.534-12597del
ENST00000474727.2:c.*145-12597del	ENSP00000419090.2:n.*145-12597del
NM_173653.3:c.534-12597del	NP_775924.1:n.534-12597del
XM_011512704.1:c.534-12597del	XP_011511006.1:n.534-12597del
XM_011512704.3:c.534-12597del	XP_011511006.1:n.534-12597del
XM_017006202.2:c.534-12597del	XP_016861691.1:n.534-12597del
XM_017006203.1:c.183-12597del	XP_016861692.1:n.183-12597del
NM_173653.4:c.534-12597del MANE Select	NP_775924.1:n.534-12597del