Canonical Allele Identifier: CA1407535411
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143705928C= , CM000665.2:g.143705928C= GRCh38
NC_000003.11:g.143424770C= , CM000665.1:g.143424770C= GRCh37
NC_000003.10:g.144907460C= NCBI36
NG_017077.1:g.147604G=
NG_017077.2:g.147604G=

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.534-12621G= MANE Select ENSP00000320246.6:n.534-12621G=
ENST00000316549.10:c.534-12621G= ENSP00000320246.6:n.534-12621G=
ENST00000474727.2:c.*145-12621G= ENSP00000419090.2:n.*145-12621G=
NM_173653.3:c.534-12621G= NP_775924.1:n.534-12621G=
XM_011512704.1:c.534-12621G= XP_011511006.1:n.534-12621G=
XM_011512704.3:c.534-12621G= XP_011511006.1:n.534-12621G=
XM_017006202.2:c.534-12621G= XP_016861691.1:n.534-12621G=
XM_017006203.1:c.183-12621G= XP_016861692.1:n.183-12621G=
NM_173653.4:c.534-12621G= MANE Select NP_775924.1:n.534-12621G=