Canonical Allele Identifier: CA1407372373
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143337613T= , CM000665.2:g.143337613T= GRCh38
NC_000003.11:g.143056455T= , CM000665.1:g.143056455T= GRCh37
NC_000003.10:g.144539145T= NCBI36
NG_017077.1:g.515919A=
NG_017077.2:g.515919A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.1604+25871A= MANE Select ENSP00000320246.6:n.1604+25871A=
ENST00000316549.10:c.1604+25871A= ENSP00000320246.6:n.1604+25871A=
NM_173653.3:c.1604+25871A= NP_775924.1:n.1604+25871A=
XM_011512703.1:c.956+25871A= XP_011511005.1:n.956+25871A=
XM_011512703.3:c.956+25871A= XP_011511005.1:n.956+25871A=
XM_017006202.2:c.1711+25764A= XP_016861691.1:n.1711+25764A=
XM_017006203.1:c.1253+25871A= XP_016861692.1:n.1253+25871A=
NM_173653.4:c.1604+25871A= MANE Select NP_775924.1:n.1604+25871A=