Canonical Allele Identifier: CA1407372336
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143337530C= , CM000665.2:g.143337530C= GRCh38
NC_000003.11:g.143056372C= , CM000665.1:g.143056372C= GRCh37
NC_000003.10:g.144539062C= NCBI36
NG_017077.1:g.516002G=
NG_017077.2:g.516002G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.1604+25954G= MANE Select ENSP00000320246.6:n.1604+25954G=
ENST00000316549.10:c.1604+25954G= ENSP00000320246.6:n.1604+25954G=
NM_173653.3:c.1604+25954G= NP_775924.1:n.1604+25954G=
XM_011512703.1:c.956+25954G= XP_011511005.1:n.956+25954G=
XM_011512703.3:c.956+25954G= XP_011511005.1:n.956+25954G=
XM_017006202.2:c.1711+25847G= XP_016861691.1:n.1711+25847G=
XM_017006203.1:c.1253+25954G= XP_016861692.1:n.1253+25954G=
NM_173653.4:c.1604+25954G= MANE Select NP_775924.1:n.1604+25954G=