Canonical Allele Identifier: CA1884371329

Gene: SLC34A3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137234634C= , CM000671.2:g.137234634C=	GRCh38
NC_000009.11:g.140129086C= , CM000671.1:g.140129086C=	GRCh37
NC_000009.10:g.139248907C=	NCBI36
NG_017008.1:g.8878C=
NG_017008.2:g.8734C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001177316.2:c.1238C= MANE Select	NP_001170787.2:p.Ala413=
ENST00000673835.1:c.1238C= MANE Select	ENSP00000501114.1:p.Ala413=
NM_001177316.1:c.1238C=	NP_001170787.1:p.Ala413=
NM_001177317.1:c.1238C=	NP_001170788.1:p.Ala413=
NM_001177317.2:c.1238C=	NP_001170788.2:p.Ala413=
NM_080877.2:c.1238C=	NP_543153.1:p.Ala413=
NM_080877.3:c.1238C=	NP_543153.2:p.Ala413=
ENST00000361134.2:c.1238C=	ENSP00000355353.2:p.Ala413=
ENST00000538474.5:c.1238C=	ENSP00000442397.1:p.Ala413=
XM_011518256.1:c.1238C=	XP_011516558.1:p.Ala413=
XM_011518257.1:c.1238C=	XP_011516559.1:p.Ala413=
XM_011518257.2:c.1238C=	XP_011516559.1:p.Ala413=
XM_011518258.1:c.1238C=	XP_011516560.1:p.Ala413=
XM_011518259.1:c.1238C=	XP_011516561.1:p.Ala413=
XM_011518260.1:c.1238C=	XP_011516562.1:p.Ala413=
XM_011518261.1:c.1238C=	XP_011516563.1:p.Ala413=
XM_011518261.2:c.1238C=	XP_011516563.1:p.Ala413=
XM_011518262.1:c.1238C=	XP_011516564.1:p.Ala413=
XM_017014290.1:c.1238C=	XP_016869779.1:p.Ala413=
XM_017014291.1:c.1238C=	XP_016869780.1:p.Ala413=
XM_017014292.1:c.1238C=	XP_016869781.1:p.Ala413=