Canonical Allele Identifier: CA1407372310
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143337479G= , CM000665.2:g.143337479G= GRCh38
NC_000003.11:g.143056321G= , CM000665.1:g.143056321G= GRCh37
NC_000003.10:g.144539011G= NCBI36
NG_017077.1:g.516053C=
NG_017077.2:g.516053C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.1604+26005C= MANE Select ENSP00000320246.6:n.1604+26005C=
ENST00000316549.10:c.1604+26005C= ENSP00000320246.6:n.1604+26005C=
NM_173653.3:c.1604+26005C= NP_775924.1:n.1604+26005C=
XM_011512703.1:c.956+26005C= XP_011511005.1:n.956+26005C=
XM_011512703.3:c.956+26005C= XP_011511005.1:n.956+26005C=
XM_017006202.2:c.1711+25898C= XP_016861691.1:n.1711+25898C=
XM_017006203.1:c.1253+26005C= XP_016861692.1:n.1253+26005C=
NM_173653.4:c.1604+26005C= MANE Select NP_775924.1:n.1604+26005C=