Canonical Allele Identifier: CA1407372380
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143337625G= , CM000665.2:g.143337625G= GRCh38
NC_000003.11:g.143056467G= , CM000665.1:g.143056467G= GRCh37
NC_000003.10:g.144539157G= NCBI36
NG_017077.1:g.515907C=
NG_017077.2:g.515907C=

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.1604+25859C= MANE Select ENSP00000320246.6:n.1604+25859C=
ENST00000316549.10:c.1604+25859C= ENSP00000320246.6:n.1604+25859C=
NM_173653.3:c.1604+25859C= NP_775924.1:n.1604+25859C=
XM_011512703.1:c.956+25859C= XP_011511005.1:n.956+25859C=
XM_011512703.3:c.956+25859C= XP_011511005.1:n.956+25859C=
XM_017006202.2:c.1711+25752C= XP_016861691.1:n.1711+25752C=
XM_017006203.1:c.1253+25859C= XP_016861692.1:n.1253+25859C=
NM_173653.4:c.1604+25859C= MANE Select NP_775924.1:n.1604+25859C=