Canonical Allele Identifier: CA1054439556
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs1934013532

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143707399del , CM000665.2:g.143707399del GRCh38
NC_000003.11:g.143426241del , CM000665.1:g.143426241del GRCh37
NC_000003.10:g.144908931del NCBI36
NG_017077.1:g.146133del
NG_017077.2:g.146133del

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.534-14092del MANE Select ENSP00000320246.6:n.534-14092del
ENST00000316549.10:c.534-14092del ENSP00000320246.6:n.534-14092del
ENST00000474727.2:c.*145-14092del ENSP00000419090.2:n.*145-14092del
NM_173653.3:c.534-14092del NP_775924.1:n.534-14092del
XM_011512704.1:c.534-14092del XP_011511006.1:n.534-14092del
XM_011512704.3:c.534-14092del XP_011511006.1:n.534-14092del
XM_017006202.2:c.534-14092del XP_016861691.1:n.534-14092del
XM_017006203.1:c.183-14092del XP_016861692.1:n.183-14092del
NM_173653.4:c.534-14092del MANE Select NP_775924.1:n.534-14092del