Canonical Allele Identifier: CA1407455104
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143531200C= , CM000665.2:g.143531200C= GRCh38
NC_000003.11:g.143250042C= , CM000665.1:g.143250042C= GRCh37
NC_000003.10:g.144732732C= NCBI36
NG_017077.1:g.322332G=
NG_017077.2:g.322332G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.1089+21162G= MANE Select ENSP00000320246.6:n.1089+21162G=
ENST00000316549.10:c.1089+21162G= ENSP00000320246.6:n.1089+21162G=
NM_173653.3:c.1089+21162G= NP_775924.1:n.1089+21162G=
XM_011512703.1:c.441+21162G= XP_011511005.1:n.441+21162G=
XM_011512703.3:c.441+21162G= XP_011511005.1:n.441+21162G=
XM_017006202.2:c.1089+21162G= XP_016861691.1:n.1089+21162G=
XM_017006203.1:c.738+21162G= XP_016861692.1:n.738+21162G=
NM_173653.4:c.1089+21162G= MANE Select NP_775924.1:n.1089+21162G=