Canonical Allele Identifier: CA1407372314

Gene: SLC9A9

Linked Data

• dbSNP Id: rs2031963650

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143337482_143337484dup , CM000665.2:g.143337482_143337484dup	GRCh38
NC_000003.11:g.143056324_143056326dup , CM000665.1:g.143056324_143056326dup	GRCh37
NC_000003.10:g.144539014_144539016dup	NCBI36
NG_017077.1:g.516049_516051dup
NG_017077.2:g.516049_516051dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1604+26001_1604+26003dup MANE Select	ENSP00000320246.6:n.1604+26001_1604+26003dup
ENST00000316549.10:c.1604+26001_1604+26003dup	ENSP00000320246.6:n.1604+26001_1604+26003dup
NM_173653.3:c.1604+26001_1604+26003dup	NP_775924.1:n.1604+26001_1604+26003dup
XM_011512703.1:c.956+26001_956+26003dup	XP_011511005.1:n.956+26001_956+26003dup
XM_011512703.3:c.956+26001_956+26003dup	XP_011511005.1:n.956+26001_956+26003dup
XM_017006202.2:c.1711+25894_1711+25896dup	XP_016861691.1:n.1711+25894_1711+25896dup
XM_017006203.1:c.1253+26001_1253+26003dup	XP_016861692.1:n.1253+26001_1253+26003dup
NM_173653.4:c.1604+26001_1604+26003dup MANE Select	NP_775924.1:n.1604+26001_1604+26003dup