Canonical Allele Identifier: CA1407354919
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143302130A= , CM000665.2:g.143302130A= GRCh38
NC_000003.11:g.143020972A= , CM000665.1:g.143020972A= GRCh37
NC_000003.10:g.144503662A= NCBI36
NG_017077.1:g.551402T=
NG_017077.2:g.551402T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.1605-33150T= MANE Select ENSP00000320246.6:n.1605-33150T=
ENST00000316549.10:c.1605-33150T= ENSP00000320246.6:n.1605-33150T=
NM_173653.3:c.1605-33150T= NP_775924.1:n.1605-33150T=
XM_011512703.1:c.957-33150T= XP_011511005.1:n.957-33150T=
XM_011512703.3:c.957-33150T= XP_011511005.1:n.957-33150T=
XM_017006202.2:c.1712-17788T= XP_016861691.1:n.1712-17788T=
XM_017006203.1:c.1254-33150T= XP_016861692.1:n.1254-33150T=
NM_173653.4:c.1605-33150T= MANE Select NP_775924.1:n.1605-33150T=