Canonical Allele Identifier: CA85222836

Gene: SLC9A9

Linked Data

• dbSNP Id: rs753929865
• gnomAD v2: 3-143056406-AC-A
• gnomAD v3: 3-143337564-AC-A
• gnomAD v4: 3-143337564-AC-A
• MyVariant Identifiers: chr3:g.143056407del (hg19) ; chr3:g.143337565del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143337566del , CM000665.2:g.143337566del	GRCh38
NC_000003.11:g.143056408del , CM000665.1:g.143056408del	GRCh37
NC_000003.10:g.144539098del	NCBI36
NG_017077.1:g.515967del
NG_017077.2:g.515967del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1604+25919del MANE Select	ENSP00000320246.6:n.1604+25919del
ENST00000316549.10:c.1604+25919del	ENSP00000320246.6:n.1604+25919del
NM_173653.3:c.1604+25919del	NP_775924.1:n.1604+25919del
XM_011512703.1:c.956+25919del	XP_011511005.1:n.956+25919del
XM_011512703.3:c.956+25919del	XP_011511005.1:n.956+25919del
XM_017006202.2:c.1711+25812del	XP_016861691.1:n.1711+25812del
XM_017006203.1:c.1253+25919del	XP_016861692.1:n.1253+25919del
NM_173653.4:c.1604+25919del MANE Select	NP_775924.1:n.1604+25919del