Canonical Allele Identifier: CA1407529449
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143693258del , CM000665.2:g.143693258del GRCh38
NC_000003.11:g.143412100del , CM000665.1:g.143412100del GRCh37
NC_000003.10:g.144894790del NCBI36
NG_017077.1:g.160278del
NG_017077.2:g.160278del

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.587del MANE Select ENSP00000320246.6:p.Asn196MetfsTer15
ENST00000316549.10:c.587del ENSP00000320246.6:p.Asn196MetfsTer15
ENST00000474727.2:c.*198del ENSP00000419090.2:n.*198del
ENST00000483124.1:n.124del
NM_173653.3:c.587del NP_775924.1:p.Asn196MetfsTer15
XM_011512703.1:c.-160del XP_011511005.1:n.-160del
XM_011512704.1:c.587del XP_011511006.1:p.Asn196MetfsTer15
XM_011512703.3:c.-160del XP_011511005.1:n.-160del
XM_011512704.3:c.587del XP_011511006.1:p.Asn196MetfsTer15
XM_017006202.2:c.587del XP_016861691.1:p.Asn196MetfsTer15
XM_017006203.1:c.236del XP_016861692.1:p.Asn79MetfsTer15
NM_173653.4:c.587del MANE Select NP_775924.1:p.Asn196MetfsTer15