Canonical Allele Identifier: CA216289
Gene: SLC34A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 64502
ClinVar RCV Id: RCV000054689
dbSNP Id: rs387907510

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137233027C>T , CM000671.2:g.137233027C>T GRCh38
NC_000009.11:g.140127479C>T , CM000671.1:g.140127479C>T GRCh37
NC_000009.10:g.139247300C>T NCBI36
NG_017008.1:g.7271C>T
NG_017008.2:g.7127C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000673835.1:c.472C>T MANE Select ENSP00000501114.1:p.Pro158Ser
ENST00000673865.1:c.472C>T ENSP00000501101.1:p.Pro158Ser
ENST00000361134.2:c.472C>T ENSP00000355353.2:p.Pro158Ser
ENST00000538474.5:c.472C>T ENSP00000442397.1:p.Pro158Ser
NM_001177316.1:c.472C>T NP_001170787.1:p.Pro158Ser
NM_001177317.1:c.472C>T NP_001170788.1:p.Pro158Ser
NM_080877.2:c.472C>T NP_543153.1:p.Pro158Ser
XM_011518256.1:c.472C>T XP_011516558.1:p.Pro158Ser
XM_011518257.1:c.472C>T XP_011516559.1:p.Pro158Ser
XM_011518258.1:c.472C>T XP_011516560.1:p.Pro158Ser
XM_011518259.1:c.472C>T XP_011516561.1:p.Pro158Ser
XM_011518260.1:c.472C>T XP_011516562.1:p.Pro158Ser
XM_011518261.1:c.472C>T XP_011516563.1:p.Pro158Ser
XM_011518262.1:c.472C>T XP_011516564.1:p.Pro158Ser
XM_011518257.2:c.472C>T XP_011516559.1:p.Pro158Ser
XM_011518261.2:c.472C>T XP_011516563.1:p.Pro158Ser
XM_017014290.1:c.472C>T XP_016869779.1:p.Pro158Ser
XM_017014291.1:c.472C>T XP_016869780.1:p.Pro158Ser
XM_017014292.1:c.472C>T XP_016869781.1:p.Pro158Ser
NM_001177316.2:c.472C>T MANE Select NP_001170787.2:p.Pro158Ser
NM_001177317.2:c.472C>T NP_001170788.2:p.Pro158Ser
NM_080877.3:c.472C>T NP_543153.2:p.Pro158Ser