Canonical Allele Identifier: CA1407536492

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707051_143707055delinsAAGTG , CM000665.2:g.143707051_143707055delinsAAGTG	GRCh38
NC_000003.11:g.143425893_143425897delinsAAGTG , CM000665.1:g.143425893_143425897delinsAAGTG	GRCh37
NC_000003.10:g.144908583_144908587delinsAAGTG	NCBI36
NG_017077.1:g.146477_146481delinsCACTT
NG_017077.2:g.146477_146481delinsCACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-13748_534-13744delinsCACTT MANE Select	ENSP00000320246.6:n.534-13748_534-13744delinsCACTT
ENST00000316549.10:c.534-13748_534-13744delinsCACTT	ENSP00000320246.6:n.534-13748_534-13744delinsCACTT
ENST00000474727.2:c.*145-13748_*145-13744delinsCACTT	ENSP00000419090.2:n.*145-13748_*145-13744delinsCACTT
NM_173653.3:c.534-13748_534-13744delinsCACTT	NP_775924.1:n.534-13748_534-13744delinsCACTT
XM_011512704.1:c.534-13748_534-13744delinsCACTT	XP_011511006.1:n.534-13748_534-13744delinsCACTT
XM_011512704.3:c.534-13748_534-13744delinsCACTT	XP_011511006.1:n.534-13748_534-13744delinsCACTT
XM_017006202.2:c.534-13748_534-13744delinsCACTT	XP_016861691.1:n.534-13748_534-13744delinsCACTT
XM_017006203.1:c.183-13748_183-13744delinsCACTT	XP_016861692.1:n.183-13748_183-13744delinsCACTT
NM_173653.4:c.534-13748_534-13744delinsCACTT MANE Select	NP_775924.1:n.534-13748_534-13744delinsCACTT