Canonical Allele Identifier: CA1407536787

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707384_143707385delinsAC , CM000665.2:g.143707384_143707385delinsAC	GRCh38
NC_000003.11:g.143426226_143426227delinsAC , CM000665.1:g.143426226_143426227delinsAC	GRCh37
NC_000003.10:g.144908916_144908917delinsAC	NCBI36
NG_017077.1:g.146147_146148delinsGT
NG_017077.2:g.146147_146148delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-14078_534-14077delinsGT MANE Select	ENSP00000320246.6:n.534-14078_534-14077delinsGT
ENST00000316549.10:c.534-14078_534-14077delinsGT	ENSP00000320246.6:n.534-14078_534-14077delinsGT
ENST00000474727.2:c.*145-14078_*145-14077delinsGT	ENSP00000419090.2:n.*145-14078_*145-14077delinsGT
NM_173653.3:c.534-14078_534-14077delinsGT	NP_775924.1:n.534-14078_534-14077delinsGT
XM_011512704.1:c.534-14078_534-14077delinsGT	XP_011511006.1:n.534-14078_534-14077delinsGT
XM_011512704.3:c.534-14078_534-14077delinsGT	XP_011511006.1:n.534-14078_534-14077delinsGT
XM_017006202.2:c.534-14078_534-14077delinsGT	XP_016861691.1:n.534-14078_534-14077delinsGT
XM_017006203.1:c.183-14078_183-14077delinsGT	XP_016861692.1:n.183-14078_183-14077delinsGT
NM_173653.4:c.534-14078_534-14077delinsGT MANE Select	NP_775924.1:n.534-14078_534-14077delinsGT