Canonical Allele Identifier: CA1407352426
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143286061_143286066delinsATTCTC , CM000665.2:g.143286061_143286066delinsATTCTC GRCh38
NC_000003.11:g.143004903_143004908delinsATTCTC , CM000665.1:g.143004903_143004908delinsATTCTC GRCh37
NC_000003.10:g.144487593_144487598delinsATTCTC NCBI36
NG_017077.1:g.567466_567471delinsGAGAAT
NG_017077.2:g.567466_567471delinsGAGAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.1605-17086_1605-17081delinsGAGAAT MANE Select ENSP00000320246.6:n.1605-17086_1605-17081delinsGAGAAT
ENST00000316549.10:c.1605-17086_1605-17081delinsGAGAAT ENSP00000320246.6:n.1605-17086_1605-17081delinsGAGAAT
NM_173653.3:c.1605-17086_1605-17081delinsGAGAAT NP_775924.1:n.1605-17086_1605-17081delinsGAGAAT
XM_011512703.1:c.957-17086_957-17081delinsGAGAAT XP_011511005.1:n.957-17086_957-17081delinsGAGAAT
XM_011512703.3:c.957-17086_957-17081delinsGAGAAT XP_011511005.1:n.957-17086_957-17081delinsGAGAAT
XM_017006202.2:c.1712-1724_1712-1719delinsGAGAAT XP_016861691.1:n.1712-1724_1712-1719delinsGAGAAT
XM_017006203.1:c.1254-17086_1254-17081delinsGAGAAT XP_016861692.1:n.1254-17086_1254-17081delinsGAGAAT
NM_173653.4:c.1605-17086_1605-17081delinsGAGAAT MANE Select NP_775924.1:n.1605-17086_1605-17081delinsGAGAAT