Canonical Allele Identifier: CA85301678

Gene: SLC9A9

Linked Data

• dbSNP Id: rs972258179
• gnomAD v2: 3-143424605-CTT-C
• gnomAD v3: 3-143705763-CTT-C
• gnomAD v4: 3-143705763-CTT-C
• MyVariant Identifiers: chr3:g.143424606_143424607del (hg19) ; chr3:g.143705764_143705765del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143705765_143705766del , CM000665.2:g.143705765_143705766del	GRCh38
NC_000003.11:g.143424607_143424608del , CM000665.1:g.143424607_143424608del	GRCh37
NC_000003.10:g.144907297_144907298del	NCBI36
NG_017077.1:g.147767_147768del
NG_017077.2:g.147767_147768del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-12458_534-12457del MANE Select	ENSP00000320246.6:n.534-12458_534-12457del
ENST00000316549.10:c.534-12458_534-12457del	ENSP00000320246.6:n.534-12458_534-12457del
ENST00000474727.2:c.*145-12458_*145-12457del	ENSP00000419090.2:n.*145-12458_*145-12457del
NM_173653.3:c.534-12458_534-12457del	NP_775924.1:n.534-12458_534-12457del
XM_011512704.1:c.534-12458_534-12457del	XP_011511006.1:n.534-12458_534-12457del
XM_011512704.3:c.534-12458_534-12457del	XP_011511006.1:n.534-12458_534-12457del
XM_017006202.2:c.534-12458_534-12457del	XP_016861691.1:n.534-12458_534-12457del
XM_017006203.1:c.183-12458_183-12457del	XP_016861692.1:n.183-12458_183-12457del
NM_173653.4:c.534-12458_534-12457del MANE Select	NP_775924.1:n.534-12458_534-12457del