Canonical Allele Identifier: CA201700167

Gene: SLC34A3

Linked Data

• dbSNP Id: rs201678672
• MyVariant Identifiers: chr9:g.140130684C>G (hg19) ; chr9:g.137236232C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137236232C>G , CM000671.2:g.137236232C>G	GRCh38
NC_000009.11:g.140130684C>G , CM000671.1:g.140130684C>G	GRCh37
NC_000009.10:g.139250505C>G	NCBI36
NG_017008.1:g.10476C>G
NG_017008.2:g.10332C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673835.1:c.1616C>G MANE Select	ENSP00000501114.1:p.Pro539Arg
ENST00000361134.2:c.1616C>G	ENSP00000355353.2:p.Pro539Arg
ENST00000538474.5:c.1616C>G	ENSP00000442397.1:p.Pro539Arg
NM_001177316.1:c.1616C>G	NP_001170787.1:p.Pro539Arg
NM_001177317.1:c.1616C>G	NP_001170788.1:p.Pro539Arg
NM_080877.2:c.1616C>G	NP_543153.1:p.Pro539Arg
XM_017014292.1:c.1616C>G	XP_016869781.1:p.Pro539Arg
NM_001177316.2:c.1616C>G MANE Select	NP_001170787.2:p.Pro539Arg
NM_001177317.2:c.1616C>G	NP_001170788.2:p.Pro539Arg
NM_080877.3:c.1616C>G	NP_543153.2:p.Pro539Arg