Canonical Allele Identifier: CA467942664
Gene: SLC34A3 HGNC NCBI

Linked Data

dbSNP Id: rs1836584325
MyVariant Identifiers: chr9:g.140130640G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137236188G>A , CM000671.2:g.137236188G>A GRCh38
NC_000009.11:g.140130640G>A , CM000671.1:g.140130640G>A GRCh37
NC_000009.10:g.139250461G>A NCBI36
NG_017008.1:g.10432G>A
NG_017008.2:g.10288G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000673835.1:c.1572G>A MANE Select ENSP00000501114.1:p.Leu524=
ENST00000361134.2:c.1572G>A ENSP00000355353.2:p.Leu524=
ENST00000538474.5:c.1572G>A ENSP00000442397.1:p.Leu524=
NM_001177316.1:c.1572G>A NP_001170787.1:p.Leu524=
NM_001177317.1:c.1572G>A NP_001170788.1:p.Leu524=
NM_080877.2:c.1572G>A NP_543153.1:p.Leu524=
XM_017014292.1:c.1572G>A XP_016869781.1:p.Leu524=
NM_001177316.2:c.1572G>A MANE Select NP_001170787.2:p.Leu524=
NM_001177317.2:c.1572G>A NP_001170788.2:p.Leu524=
NM_080877.3:c.1572G>A NP_543153.2:p.Leu524=