Canonical Allele Identifier: CA1407372318

Gene: SLC9A9

Linked Data

• dbSNP Id: rs2031964532

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143337493_143337496dup , CM000665.2:g.143337493_143337496dup	GRCh38
NC_000003.11:g.143056335_143056338dup , CM000665.1:g.143056335_143056338dup	GRCh37
NC_000003.10:g.144539025_144539028dup	NCBI36
NG_017077.1:g.516039_516042dup
NG_017077.2:g.516039_516042dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1604+25991_1604+25994dup MANE Select	ENSP00000320246.6:n.1604+25991_1604+25994dup
ENST00000316549.10:c.1604+25991_1604+25994dup	ENSP00000320246.6:n.1604+25991_1604+25994dup
NM_173653.3:c.1604+25991_1604+25994dup	NP_775924.1:n.1604+25991_1604+25994dup
XM_011512703.1:c.956+25991_956+25994dup	XP_011511005.1:n.956+25991_956+25994dup
XM_011512703.3:c.956+25991_956+25994dup	XP_011511005.1:n.956+25991_956+25994dup
XM_017006202.2:c.1711+25884_1711+25887dup	XP_016861691.1:n.1711+25884_1711+25887dup
XM_017006203.1:c.1253+25991_1253+25994dup	XP_016861692.1:n.1253+25991_1253+25994dup
NM_173653.4:c.1604+25991_1604+25994dup MANE Select	NP_775924.1:n.1604+25991_1604+25994dup