Canonical Allele Identifier: CA2758721756

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143337614_143337615insCACT , CM000665.2:g.143337614_143337615insCACT	GRCh38
NC_000003.11:g.143056456_143056457insCACT , CM000665.1:g.143056456_143056457insCACT	GRCh37
NC_000003.10:g.144539146_144539147insCACT	NCBI36
NG_017077.1:g.515918_515919insGTGA
NG_017077.2:g.515918_515919insGTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1604+25870_1604+25871insGTGA MANE Select	ENSP00000320246.6:n.1604+25870_1604+25871insGTGA
ENST00000316549.10:c.1604+25870_1604+25871insGTGA	ENSP00000320246.6:n.1604+25870_1604+25871insGTGA
NM_173653.3:c.1604+25870_1604+25871insGTGA	NP_775924.1:n.1604+25870_1604+25871insGTGA
XM_011512703.1:c.956+25870_956+25871insGTGA	XP_011511005.1:n.956+25870_956+25871insGTGA
XM_011512703.3:c.956+25870_956+25871insGTGA	XP_011511005.1:n.956+25870_956+25871insGTGA
XM_017006202.2:c.1711+25763_1711+25764insGTGA	XP_016861691.1:n.1711+25763_1711+25764insGTGA
XM_017006203.1:c.1253+25870_1253+25871insGTGA	XP_016861692.1:n.1253+25870_1253+25871insGTGA
NM_173653.4:c.1604+25870_1604+25871insGTGA MANE Select	NP_775924.1:n.1604+25870_1604+25871insGTGA