Canonical Allele Identifier: CA16609447
Gene: SLC34A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 397583
ClinVar RCV Id: RCV000449572
dbSNP Id: rs1060499697
MyVariant Identifiers: chr9:g.140129122C>T (hg19) chr9:g.137234670C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137234670C>T , CM000671.2:g.137234670C>T GRCh38
NC_000009.11:g.140129122C>T , CM000671.1:g.140129122C>T GRCh37
NC_000009.10:g.139248943C>T NCBI36
NG_017008.1:g.8914C>T
NG_017008.2:g.8770C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000673835.1:c.1274C>T MANE Select ENSP00000501114.1:p.Thr425Ile
ENST00000361134.2:c.1274C>T ENSP00000355353.2:p.Thr425Ile
ENST00000538474.5:c.1274C>T ENSP00000442397.1:p.Thr425Ile
NM_001177316.1:c.1274C>T NP_001170787.1:p.Thr425Ile
NM_001177317.1:c.1274C>T NP_001170788.1:p.Thr425Ile
NM_080877.2:c.1274C>T NP_543153.1:p.Thr425Ile
XM_011518256.1:c.1274C>T XP_011516558.1:p.Thr425Ile
XM_011518257.1:c.1274C>T XP_011516559.1:p.Thr425Ile
XM_011518258.1:c.1274C>T XP_011516560.1:p.Thr425Ile
XM_011518259.1:c.1274C>T XP_011516561.1:p.Thr425Ile
XM_011518260.1:c.1274C>T XP_011516562.1:p.Thr425Ile
XM_011518261.1:c.1274C>T XP_011516563.1:p.Thr425Ile
XM_011518262.1:c.1274C>T XP_011516564.1:p.Thr425Ile
XM_011518257.2:c.1274C>T XP_011516559.1:p.Thr425Ile
XM_011518261.2:c.1274C>T XP_011516563.1:p.Thr425Ile
XM_017014290.1:c.1274C>T XP_016869779.1:p.Thr425Ile
XM_017014291.1:c.1274C>T XP_016869780.1:p.Thr425Ile
XM_017014292.1:c.1274C>T XP_016869781.1:p.Thr425Ile
NM_001177316.2:c.1274C>T MANE Select NP_001170787.2:p.Thr425Ile
NM_001177317.2:c.1274C>T NP_001170788.2:p.Thr425Ile
NM_080877.3:c.1274C>T NP_543153.2:p.Thr425Ile
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