Canonical Allele Identifier: CA1407535398
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143705903_143705904delinsGA , CM000665.2:g.143705903_143705904delinsGA GRCh38
NC_000003.11:g.143424745_143424746delinsGA , CM000665.1:g.143424745_143424746delinsGA GRCh37
NC_000003.10:g.144907435_144907436delinsGA NCBI36
NG_017077.1:g.147628_147629delinsTC
NG_017077.2:g.147628_147629delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.534-12597_534-12596delinsTC MANE Select ENSP00000320246.6:n.534-12597_534-12596de...
ENST00000316549.10:c.534-12597_534-12596delinsTC ENSP00000320246.6:n.534-12597_534-12596de...
ENST00000474727.2:c.*145-12597_*145-12596delinsTC ENSP00000419090.2:n.*145-12597_*145-12596...
NM_173653.3:c.534-12597_534-12596delinsTC NP_775924.1:n.534-12597_534-12596delinsTC...
XM_011512704.1:c.534-12597_534-12596delinsTC XP_011511006.1:n.534-12597_534-12596delin...
XM_011512704.3:c.534-12597_534-12596delinsTC XP_011511006.1:n.534-12597_534-12596delin...
XM_017006202.2:c.534-12597_534-12596delinsTC XP_016861691.1:n.534-12597_534-12596delin...
XM_017006203.1:c.183-12597_183-12596delinsTC XP_016861692.1:n.183-12597_183-12596delin...
NM_173653.4:c.534-12597_534-12596delinsTC MANE Select NP_775924.1:n.534-12597_534-12596delinsTC...