Canonical Allele Identifier: CA1884372230
Gene: SLC34A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137236174C= , CM000671.2:g.137236174C= GRCh38
NC_000009.11:g.140130626C= , CM000671.1:g.140130626C= GRCh37
NC_000009.10:g.139250447C= NCBI36
NG_017008.1:g.10418C=
NG_017008.2:g.10274C=

Transcript Alleles

HGVS Amino-acid change
ENST00000673835.1:c.1558C= MANE Select ENSP00000501114.1:p.Pro520=
ENST00000361134.2:c.1558C= ENSP00000355353.2:p.Pro520=
ENST00000538474.5:c.1558C= ENSP00000442397.1:p.Pro520=
NM_001177316.1:c.1558C= NP_001170787.1:p.Pro520=
NM_001177317.1:c.1558C= NP_001170788.1:p.Pro520=
NM_080877.2:c.1558C= NP_543153.1:p.Pro520=
XM_017014292.1:c.1558C= XP_016869781.1:p.Pro520=
NM_001177316.2:c.1558C= MANE Select NP_001170787.2:p.Pro520=
NM_001177317.2:c.1558C= NP_001170788.2:p.Pro520=
NM_080877.3:c.1558C= NP_543153.2:p.Pro520=