Canonical Allele Identifier: CA1407536528
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143707096C= , CM000665.2:g.143707096C= GRCh38
NC_000003.11:g.143425938C= , CM000665.1:g.143425938C= GRCh37
NC_000003.10:g.144908628C= NCBI36
NG_017077.1:g.146436G=
NG_017077.2:g.146436G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.534-13789G= MANE Select ENSP00000320246.6:n.534-13789G=
ENST00000316549.10:c.534-13789G= ENSP00000320246.6:n.534-13789G=
ENST00000474727.2:c.*145-13789G= ENSP00000419090.2:n.*145-13789G=
NM_173653.3:c.534-13789G= NP_775924.1:n.534-13789G=
XM_011512704.1:c.534-13789G= XP_011511006.1:n.534-13789G=
XM_011512704.3:c.534-13789G= XP_011511006.1:n.534-13789G=
XM_017006202.2:c.534-13789G= XP_016861691.1:n.534-13789G=
XM_017006203.1:c.183-13789G= XP_016861692.1:n.183-13789G=
NM_173653.4:c.534-13789G= MANE Select NP_775924.1:n.534-13789G=