Canonical Allele Identifier: CA1407535391
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs1933957257
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143705893_143705897del , CM000665.2:g.143705893_143705897del GRCh38
NC_000003.11:g.143424735_143424739del , CM000665.1:g.143424735_143424739del GRCh37
NC_000003.10:g.144907425_144907429del NCBI36
NG_017077.1:g.147635_147639del
NG_017077.2:g.147635_147639del

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.534-12590_534-12586del MANE Select ENSP00000320246.6:n.534-12590_534-12586de...
ENST00000316549.10:c.534-12590_534-12586del ENSP00000320246.6:n.534-12590_534-12586de...
ENST00000474727.2:c.*145-12590_*145-12586del ENSP00000419090.2:n.*145-12590_*145-12586...
NM_173653.3:c.534-12590_534-12586del NP_775924.1:n.534-12590_534-12586del
XM_011512704.1:c.534-12590_534-12586del XP_011511006.1:n.534-12590_534-12586del
XM_011512704.3:c.534-12590_534-12586del XP_011511006.1:n.534-12590_534-12586del
XM_017006202.2:c.534-12590_534-12586del XP_016861691.1:n.534-12590_534-12586del
XM_017006203.1:c.183-12590_183-12586del XP_016861692.1:n.183-12590_183-12586del
NM_173653.4:c.534-12590_534-12586del MANE Select NP_775924.1:n.534-12590_534-12586del
Search 100 bp 5'
Search 100 bp 3'