Canonical Allele Identifier: CA1407571652

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143785734_143785738delinsCTTGG , CM000665.2:g.143785734_143785738delinsCTTGG	GRCh38
NC_000003.11:g.143504576_143504580delinsCTTGG , CM000665.1:g.143504576_143504580delinsCTTGG	GRCh37
NC_000003.10:g.144987266_144987270delinsCTTGG	NCBI36
NG_017077.1:g.67794_67798delinsCCAAG
NG_017077.2:g.67794_67798delinsCCAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.533+9263_533+9267delinsCCAAG MANE Select	ENSP00000320246.6:n.533+9263_533+9267deli...
ENST00000316549.10:c.533+9263_533+9267delinsCCAAG	ENSP00000320246.6:n.533+9263_533+9267deli...
ENST00000474727.2:c.*144+9263_*144+9267delinsCCAAG	ENSP00000419090.2:n.*144+9263_*144+9267de...
NM_173653.3:c.533+9263_533+9267delinsCCAAG	NP_775924.1:n.533+9263_533+9267delinsCCAA...
XM_011512704.1:c.533+9263_533+9267delinsCCAAG	XP_011511006.1:n.533+9263_533+9267delinsC...
XM_011512704.3:c.533+9263_533+9267delinsCCAAG	XP_011511006.1:n.533+9263_533+9267delinsC...
XM_017006202.2:c.533+9263_533+9267delinsCCAAG	XP_016861691.1:n.533+9263_533+9267delinsC...
XM_017006203.1:c.182+9263_182+9267delinsCCAAG	XP_016861692.1:n.182+9263_182+9267delinsC...
NM_173653.4:c.533+9263_533+9267delinsCCAAG MANE Select	NP_775924.1:n.533+9263_533+9267delinsCCAA...