Canonical Allele Identifier: CA1407354890
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs2030545914

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143302048del , CM000665.2:g.143302048del GRCh38
NC_000003.11:g.143020890del , CM000665.1:g.143020890del GRCh37
NC_000003.10:g.144503580del NCBI36
NG_017077.1:g.551484del
NG_017077.2:g.551484del

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.1605-33068del MANE Select ENSP00000320246.6:n.1605-33068del
ENST00000316549.10:c.1605-33068del ENSP00000320246.6:n.1605-33068del
NM_173653.3:c.1605-33068del NP_775924.1:n.1605-33068del
XM_011512703.1:c.957-33068del XP_011511005.1:n.957-33068del
XM_011512703.3:c.957-33068del XP_011511005.1:n.957-33068del
XM_017006202.2:c.1712-17706del XP_016861691.1:n.1712-17706del
XM_017006203.1:c.1254-33068del XP_016861692.1:n.1254-33068del
NM_173653.4:c.1605-33068del MANE Select NP_775924.1:n.1605-33068del