Canonical Allele Identifier: CA1054400471
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs1383688016

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143285989G>A , CM000665.2:g.143285989G>A GRCh38
NC_000003.11:g.143004831G>A , CM000665.1:g.143004831G>A GRCh37
NC_000003.10:g.144487521G>A NCBI36
NG_017077.1:g.567543C>T
NG_017077.2:g.567543C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.1605-17009C>T MANE Select ENSP00000320246.6:n.1605-17009C>T
ENST00000316549.10:c.1605-17009C>T ENSP00000320246.6:n.1605-17009C>T
NM_173653.3:c.1605-17009C>T NP_775924.1:n.1605-17009C>T
XM_011512703.1:c.957-17009C>T XP_011511005.1:n.957-17009C>T
XM_011512703.3:c.957-17009C>T XP_011511005.1:n.957-17009C>T
XM_017006202.2:c.1712-1647C>T XP_016861691.1:n.1712-1647C>T
XM_017006203.1:c.1254-17009C>T XP_016861692.1:n.1254-17009C>T
NM_173653.4:c.1605-17009C>T MANE Select NP_775924.1:n.1605-17009C>T