Canonical Allele Identifier: CA1407536566

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707142_143707143delinsAC , CM000665.2:g.143707142_143707143delinsAC	GRCh38
NC_000003.11:g.143425984_143425985delinsAC , CM000665.1:g.143425984_143425985delinsAC	GRCh37
NC_000003.10:g.144908674_144908675delinsAC	NCBI36
NG_017077.1:g.146389_146390delinsGT
NG_017077.2:g.146389_146390delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-13836_534-13835delinsGT MANE Select	ENSP00000320246.6:n.534-13836_534-13835delinsGT
ENST00000316549.10:c.534-13836_534-13835delinsGT	ENSP00000320246.6:n.534-13836_534-13835delinsGT
ENST00000474727.2:c.*145-13836_*145-13835delinsGT	ENSP00000419090.2:n.*145-13836_*145-13835delinsGT
NM_173653.3:c.534-13836_534-13835delinsGT	NP_775924.1:n.534-13836_534-13835delinsGT
XM_011512704.1:c.534-13836_534-13835delinsGT	XP_011511006.1:n.534-13836_534-13835delinsGT
XM_011512704.3:c.534-13836_534-13835delinsGT	XP_011511006.1:n.534-13836_534-13835delinsGT
XM_017006202.2:c.534-13836_534-13835delinsGT	XP_016861691.1:n.534-13836_534-13835delinsGT
XM_017006203.1:c.183-13836_183-13835delinsGT	XP_016861692.1:n.183-13836_183-13835delinsGT
NM_173653.4:c.534-13836_534-13835delinsGT MANE Select	NP_775924.1:n.534-13836_534-13835delinsGT