Canonical Allele Identifier: CA546811099

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1270276180
• gnomAD v2: 3-143005011-CTAGT-C
• gnomAD v3: 3-143286169-CTAGT-C
• gnomAD v4: 3-143286169-CTAGT-C
• MyVariant Identifiers: chr3:g.143005012_143005015del (hg19) ; chr3:g.143286170_143286173del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143286172_143286175del , CM000665.2:g.143286172_143286175del	GRCh38
NC_000003.11:g.143005014_143005017del , CM000665.1:g.143005014_143005017del	GRCh37
NC_000003.10:g.144487704_144487707del	NCBI36
NG_017077.1:g.567359_567362del
NG_017077.2:g.567359_567362del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1605-17193_1605-17190del MANE Select	ENSP00000320246.6:n.1605-17193_1605-17190del
ENST00000316549.10:c.1605-17193_1605-17190del	ENSP00000320246.6:n.1605-17193_1605-17190del
NM_173653.3:c.1605-17193_1605-17190del	NP_775924.1:n.1605-17193_1605-17190del
XM_011512703.1:c.957-17193_957-17190del	XP_011511005.1:n.957-17193_957-17190del
XM_011512703.3:c.957-17193_957-17190del	XP_011511005.1:n.957-17193_957-17190del
XM_017006202.2:c.1712-1831_1712-1828del	XP_016861691.1:n.1712-1831_1712-1828del
XM_017006203.1:c.1254-17193_1254-17190del	XP_016861692.1:n.1254-17193_1254-17190del
NM_173653.4:c.1605-17193_1605-17190del MANE Select	NP_775924.1:n.1605-17193_1605-17190del