Canonical Allele Identifier: CA1407536853

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1934015437

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707437_143707438del , CM000665.2:g.143707437_143707438del	GRCh38
NC_000003.11:g.143426279_143426280del , CM000665.1:g.143426279_143426280del	GRCh37
NC_000003.10:g.144908969_144908970del	NCBI36
NG_017077.1:g.146095_146096del
NG_017077.2:g.146095_146096del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-14130_534-14129del MANE Select	ENSP00000320246.6:n.534-14130_534-14129del
ENST00000316549.10:c.534-14130_534-14129del	ENSP00000320246.6:n.534-14130_534-14129del
ENST00000474727.2:c.*145-14130_*145-14129del	ENSP00000419090.2:n.*145-14130_*145-14129del
NM_173653.3:c.534-14130_534-14129del	NP_775924.1:n.534-14130_534-14129del
XM_011512704.1:c.534-14130_534-14129del	XP_011511006.1:n.534-14130_534-14129del
XM_011512704.3:c.534-14130_534-14129del	XP_011511006.1:n.534-14130_534-14129del
XM_017006202.2:c.534-14130_534-14129del	XP_016861691.1:n.534-14130_534-14129del
XM_017006203.1:c.183-14130_183-14129del	XP_016861692.1:n.183-14130_183-14129del
NM_173653.4:c.534-14130_534-14129del MANE Select	NP_775924.1:n.534-14130_534-14129del