Canonical Allele Identifier: CA1407536711

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1934009618

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707329_143707330del , CM000665.2:g.143707329_143707330del	GRCh38
NC_000003.11:g.143426171_143426172del , CM000665.1:g.143426171_143426172del	GRCh37
NC_000003.10:g.144908861_144908862del	NCBI36
NG_017077.1:g.146205_146206del
NG_017077.2:g.146205_146206del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-14020_534-14019del MANE Select	ENSP00000320246.6:n.534-14020_534-14019del
ENST00000316549.10:c.534-14020_534-14019del	ENSP00000320246.6:n.534-14020_534-14019del
ENST00000474727.2:c.*145-14020_*145-14019del	ENSP00000419090.2:n.*145-14020_*145-14019del
NM_173653.3:c.534-14020_534-14019del	NP_775924.1:n.534-14020_534-14019del
XM_011512704.1:c.534-14020_534-14019del	XP_011511006.1:n.534-14020_534-14019del
XM_011512704.3:c.534-14020_534-14019del	XP_011511006.1:n.534-14020_534-14019del
XM_017006202.2:c.534-14020_534-14019del	XP_016861691.1:n.534-14020_534-14019del
XM_017006203.1:c.183-14020_183-14019del	XP_016861692.1:n.183-14020_183-14019del
NM_173653.4:c.534-14020_534-14019del MANE Select	NP_775924.1:n.534-14020_534-14019del