Canonical Allele Identifier: CA375741067

Gene: SLC34A3

Linked Data

• dbSNP Id: rs1440774561
• gnomAD v2: 9-140130633-T-C
• gnomAD v4: 9-137236181-T-C
• MyVariant Identifiers: chr9:g.140130633T>C (hg19) ; chr9:g.137236181T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137236181T>C , CM000671.2:g.137236181T>C	GRCh38
NC_000009.11:g.140130633T>C , CM000671.1:g.140130633T>C	GRCh37
NC_000009.10:g.139250454T>C	NCBI36
NG_017008.1:g.10425T>C
NG_017008.2:g.10281T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673835.1:c.1565T>C MANE Select	ENSP00000501114.1:p.Val522Ala
ENST00000361134.2:c.1565T>C	ENSP00000355353.2:p.Val522Ala
ENST00000538474.5:c.1565T>C	ENSP00000442397.1:p.Val522Ala
NM_001177316.1:c.1565T>C	NP_001170787.1:p.Val522Ala
NM_001177317.1:c.1565T>C	NP_001170788.1:p.Val522Ala
NM_080877.2:c.1565T>C	NP_543153.1:p.Val522Ala
XM_017014292.1:c.1565T>C	XP_016869781.1:p.Val522Ala
NM_001177316.2:c.1565T>C MANE Select	NP_001170787.2:p.Val522Ala
NM_001177317.2:c.1565T>C	NP_001170788.2:p.Val522Ala
NM_080877.3:c.1565T>C	NP_543153.2:p.Val522Ala