Canonical Allele Identifier: CA375741020

Gene: SLC34A3

Linked Data

• ClinVar Variation Id: 1356408
• ClinVar RCV Id: RCV001870072
• dbSNP Id: rs1409293542
• MyVariant Identifiers: chr9:g.140130624G>A (hg19) ; chr9:g.137236172G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137236172G>A , CM000671.2:g.137236172G>A	GRCh38
NC_000009.11:g.140130624G>A , CM000671.1:g.140130624G>A	GRCh37
NC_000009.10:g.139250445G>A	NCBI36
NG_017008.1:g.10416G>A
NG_017008.2:g.10272G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000673835.1:c.1556G>A MANE Select	ENSP00000501114.1:p.Gly519Asp
ENST00000361134.2:c.1556G>A	ENSP00000355353.2:p.Gly519Asp
ENST00000538474.5:c.1556G>A	ENSP00000442397.1:p.Gly519Asp
NM_001177316.1:c.1556G>A	NP_001170787.1:p.Gly519Asp
NM_001177317.1:c.1556G>A	NP_001170788.1:p.Gly519Asp
NM_080877.2:c.1556G>A	NP_543153.1:p.Gly519Asp
XM_017014292.1:c.1556G>A	XP_016869781.1:p.Gly519Asp
NM_001177316.2:c.1556G>A MANE Select	NP_001170787.2:p.Gly519Asp
NM_001177317.2:c.1556G>A	NP_001170788.2:p.Gly519Asp
NM_080877.3:c.1556G>A	NP_543153.2:p.Gly519Asp