Canonical Allele Identifier: CA1407352427

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1938373110

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143286069_143286073del , CM000665.2:g.143286069_143286073del	GRCh38
NC_000003.11:g.143004911_143004915del , CM000665.1:g.143004911_143004915del	GRCh37
NC_000003.10:g.144487601_144487605del	NCBI36
NG_017077.1:g.567466_567470del
NG_017077.2:g.567466_567470del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1605-17086_1605-17082del MANE Select	ENSP00000320246.6:n.1605-17086_1605-17082del
ENST00000316549.10:c.1605-17086_1605-17082del	ENSP00000320246.6:n.1605-17086_1605-17082del
NM_173653.3:c.1605-17086_1605-17082del	NP_775924.1:n.1605-17086_1605-17082del
XM_011512703.1:c.957-17086_957-17082del	XP_011511005.1:n.957-17086_957-17082del
XM_011512703.3:c.957-17086_957-17082del	XP_011511005.1:n.957-17086_957-17082del
XM_017006202.2:c.1712-1724_1712-1720del	XP_016861691.1:n.1712-1724_1712-1720del
XM_017006203.1:c.1254-17086_1254-17082del	XP_016861692.1:n.1254-17086_1254-17082del
NM_173653.4:c.1605-17086_1605-17082del MANE Select	NP_775924.1:n.1605-17086_1605-17082del