Canonical Allele Identifier: CA1407354882
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143302032G= , CM000665.2:g.143302032G= GRCh38
NC_000003.11:g.143020874G= , CM000665.1:g.143020874G= GRCh37
NC_000003.10:g.144503564G= NCBI36
NG_017077.1:g.551500C=
NG_017077.2:g.551500C=

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.1605-33052C= MANE Select ENSP00000320246.6:n.1605-33052C=
ENST00000316549.10:c.1605-33052C= ENSP00000320246.6:n.1605-33052C=
NM_173653.3:c.1605-33052C= NP_775924.1:n.1605-33052C=
XM_011512703.1:c.957-33052C= XP_011511005.1:n.957-33052C=
XM_011512703.3:c.957-33052C= XP_011511005.1:n.957-33052C=
XM_017006202.2:c.1712-17690C= XP_016861691.1:n.1712-17690C=
XM_017006203.1:c.1254-33052C= XP_016861692.1:n.1254-33052C=
NM_173653.4:c.1605-33052C= MANE Select NP_775924.1:n.1605-33052C=