Canonical Allele Identifier: CA1884372167
Gene: SLC34A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137236076T= , CM000671.2:g.137236076T= GRCh38
NC_000009.11:g.140130528T= , CM000671.1:g.140130528T= GRCh37
NC_000009.10:g.139250349T= NCBI36
NG_017008.1:g.10320T=
NG_017008.2:g.10176T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673835.1:c.1460T= MANE Select ENSP00000501114.1:p.Val487=
ENST00000361134.2:c.1460T= ENSP00000355353.2:p.Val487=
ENST00000538474.5:c.1460T= ENSP00000442397.1:p.Val487=
NM_001177316.1:c.1460T= NP_001170787.1:p.Val487=
NM_001177317.1:c.1460T= NP_001170788.1:p.Val487=
NM_080877.2:c.1460T= NP_543153.1:p.Val487=
XM_011518262.1:c.*19T= XP_011516564.1:n.*19T=
XM_017014291.1:c.*19T= XP_016869780.1:n.*19T=
XM_017014292.1:c.1460T= XP_016869781.1:p.Val487=
NM_001177316.2:c.1460T= MANE Select NP_001170787.2:p.Val487=
NM_001177317.2:c.1460T= NP_001170788.2:p.Val487=
NM_080877.3:c.1460T= NP_543153.2:p.Val487=