Canonical Allele Identifier: CA1054439578
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs60762977

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143707404del , CM000665.2:g.143707404del GRCh38
NC_000003.11:g.143426246del , CM000665.1:g.143426246del GRCh37
NC_000003.10:g.144908936del NCBI36
NG_017077.1:g.146131del
NG_017077.2:g.146131del

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.534-14094del MANE Select ENSP00000320246.6:n.534-14094del
ENST00000316549.10:c.534-14094del ENSP00000320246.6:n.534-14094del
ENST00000474727.2:c.*145-14094del ENSP00000419090.2:n.*145-14094del
NM_173653.3:c.534-14094del NP_775924.1:n.534-14094del
XM_011512704.1:c.534-14094del XP_011511006.1:n.534-14094del
XM_011512704.3:c.534-14094del XP_011511006.1:n.534-14094del
XM_017006202.2:c.534-14094del XP_016861691.1:n.534-14094del
XM_017006203.1:c.183-14094del XP_016861692.1:n.183-14094del
NM_173653.4:c.534-14094del MANE Select NP_775924.1:n.534-14094del