Canonical Allele Identifier: CA1407536871
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143707464_143707470delinsATTAGAT , CM000665.2:g.143707464_143707470delinsATTAGAT GRCh38
NC_000003.11:g.143426306_143426312delinsATTAGAT , CM000665.1:g.143426306_143426312delinsATTAGAT GRCh37
NC_000003.10:g.144908996_144909002delinsATTAGAT NCBI36
NG_017077.1:g.146062_146068delinsATCTAAT
NG_017077.2:g.146062_146068delinsATCTAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.534-14163_534-14157delinsATCTAAT MANE Select ENSP00000320246.6:n.534-14163_534-14157delinsATCTAAT
ENST00000316549.10:c.534-14163_534-14157delinsATCTAAT ENSP00000320246.6:n.534-14163_534-14157delinsATCTAAT
ENST00000474727.2:c.*145-14163_*145-14157delinsATCTAAT ENSP00000419090.2:n.*145-14163_*145-14157delinsATCTAAT
NM_173653.3:c.534-14163_534-14157delinsATCTAAT NP_775924.1:n.534-14163_534-14157delinsATCTAAT
XM_011512704.1:c.534-14163_534-14157delinsATCTAAT XP_011511006.1:n.534-14163_534-14157delinsATCTAAT
XM_011512704.3:c.534-14163_534-14157delinsATCTAAT XP_011511006.1:n.534-14163_534-14157delinsATCTAAT
XM_017006202.2:c.534-14163_534-14157delinsATCTAAT XP_016861691.1:n.534-14163_534-14157delinsATCTAAT
XM_017006203.1:c.183-14163_183-14157delinsATCTAAT XP_016861692.1:n.183-14163_183-14157delinsATCTAAT
NM_173653.4:c.534-14163_534-14157delinsATCTAAT MANE Select NP_775924.1:n.534-14163_534-14157delinsATCTAAT