Canonical Allele Identifier: CA1054400509
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs1938379895

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143286287_143286290del , CM000665.2:g.143286287_143286290del GRCh38
NC_000003.11:g.143005129_143005132del , CM000665.1:g.143005129_143005132del GRCh37
NC_000003.10:g.144487819_144487822del NCBI36
NG_017077.1:g.567244_567247del
NG_017077.2:g.567244_567247del

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.1605-17308_1605-17305del MANE Select ENSP00000320246.6:n.1605-17308_1605-17305del
ENST00000316549.10:c.1605-17308_1605-17305del ENSP00000320246.6:n.1605-17308_1605-17305del
NM_173653.3:c.1605-17308_1605-17305del NP_775924.1:n.1605-17308_1605-17305del
XM_011512703.1:c.957-17308_957-17305del XP_011511005.1:n.957-17308_957-17305del
XM_011512703.3:c.957-17308_957-17305del XP_011511005.1:n.957-17308_957-17305del
XM_017006202.2:c.1712-1946_1712-1943del XP_016861691.1:n.1712-1946_1712-1943del
XM_017006203.1:c.1254-17308_1254-17305del XP_016861692.1:n.1254-17308_1254-17305del
NM_173653.4:c.1605-17308_1605-17305del MANE Select NP_775924.1:n.1605-17308_1605-17305del