Canonical Allele Identifier: CA375741026

Gene: SLC34A3

Linked Data

• dbSNP Id: rs1409293542
• gnomAD v2: 9-140130624-G-T
• gnomAD v3: 9-137236172-G-T
• gnomAD v4: 9-137236172-G-T
• MyVariant Identifiers: chr9:g.140130624G>T (hg19) ; chr9:g.137236172G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000673835.1:c.1556G>T MANE Select	ENSP00000501114.1:p.Gly519Val
ENST00000361134.2:c.1556G>T	ENSP00000355353.2:p.Gly519Val
ENST00000538474.5:c.1556G>T	ENSP00000442397.1:p.Gly519Val
NM_001177316.1:c.1556G>T	NP_001170787.1:p.Gly519Val
NM_001177317.1:c.1556G>T	NP_001170788.1:p.Gly519Val
NM_080877.2:c.1556G>T	NP_543153.1:p.Gly519Val
XM_017014292.1:c.1556G>T	XP_016869781.1:p.Gly519Val
NM_001177316.2:c.1556G>T MANE Select	NP_001170787.2:p.Gly519Val
NM_001177317.2:c.1556G>T	NP_001170788.2:p.Gly519Val
NM_080877.3:c.1556G>T	NP_543153.2:p.Gly519Val