Canonical Allele Identifier: CA1407354916
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143302123_143302124delinsGC , CM000665.2:g.143302123_143302124delinsGC GRCh38
NC_000003.11:g.143020965_143020966delinsGC , CM000665.1:g.143020965_143020966delinsGC GRCh37
NC_000003.10:g.144503655_144503656delinsGC NCBI36
NG_017077.1:g.551408_551409delinsGC
NG_017077.2:g.551408_551409delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.1605-33144_1605-33143delinsGC MANE Select ENSP00000320246.6:n.1605-33144_1605-33143delinsGC
ENST00000316549.10:c.1605-33144_1605-33143delinsGC ENSP00000320246.6:n.1605-33144_1605-33143delinsGC
NM_173653.3:c.1605-33144_1605-33143delinsGC NP_775924.1:n.1605-33144_1605-33143delinsGC
XM_011512703.1:c.957-33144_957-33143delinsGC XP_011511005.1:n.957-33144_957-33143delinsGC
XM_011512703.3:c.957-33144_957-33143delinsGC XP_011511005.1:n.957-33144_957-33143delinsGC
XM_017006202.2:c.1712-17782_1712-17781delinsGC XP_016861691.1:n.1712-17782_1712-17781delinsGC
XM_017006203.1:c.1254-33144_1254-33143delinsGC XP_016861692.1:n.1254-33144_1254-33143delinsGC
NM_173653.4:c.1605-33144_1605-33143delinsGC MANE Select NP_775924.1:n.1605-33144_1605-33143delinsGC