Canonical Allele Identifier: CA2692818239

Gene: SLC34A3

Linked Data

• gnomAD v4: 9-137236296-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137236299del , CM000671.2:g.137236299del	GRCh38
NC_000009.11:g.140130751del , CM000671.1:g.140130751del	GRCh37
NC_000009.10:g.139250572del	NCBI36
NG_017008.1:g.10543del
NG_017008.2:g.10399del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673835.1:c.1683del MANE Select	ENSP00000501114.1:p.Trp562GlyfsTer5
ENST00000361134.2:c.1683del	ENSP00000355353.2:p.Trp562GlyfsTer5
ENST00000538474.5:c.1683del	ENSP00000442397.1:p.Trp562GlyfsTer5
NM_001177316.1:c.1683del	NP_001170787.1:p.Trp562GlyfsTer5
NM_001177317.1:c.1683del	NP_001170788.1:p.Trp562GlyfsTer5
NM_080877.2:c.1683del	NP_543153.1:p.Trp562GlyfsTer5
XM_017014292.1:c.1683del	XP_016869781.1:p.Trp562GlyfsTer5
NM_001177316.2:c.1683del MANE Select	NP_001170787.2:p.Trp562GlyfsTer5
NM_001177317.2:c.1683del	NP_001170788.2:p.Trp562GlyfsTer5
NM_080877.3:c.1683del	NP_543153.2:p.Trp562GlyfsTer5