Canonical Allele Identifier: CA467942640

Gene: SLC34A3

Linked Data

• gnomAD v4: 9-137236173-T-C
• MyVariant Identifiers: chr9:g.140130625T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137236173T>C , CM000671.2:g.137236173T>C	GRCh38
NC_000009.11:g.140130625T>C , CM000671.1:g.140130625T>C	GRCh37
NC_000009.10:g.139250446T>C	NCBI36
NG_017008.1:g.10417T>C
NG_017008.2:g.10273T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000673835.1:c.1557T>C MANE Select	ENSP00000501114.1:p.Gly519=
ENST00000361134.2:c.1557T>C	ENSP00000355353.2:p.Gly519=
ENST00000538474.5:c.1557T>C	ENSP00000442397.1:p.Gly519=
NM_001177316.1:c.1557T>C	NP_001170787.1:p.Gly519=
NM_001177317.1:c.1557T>C	NP_001170788.1:p.Gly519=
NM_080877.2:c.1557T>C	NP_543153.1:p.Gly519=
XM_017014292.1:c.1557T>C	XP_016869781.1:p.Gly519=
NM_001177316.2:c.1557T>C MANE Select	NP_001170787.2:p.Gly519=
NM_001177317.2:c.1557T>C	NP_001170788.2:p.Gly519=
NM_080877.3:c.1557T>C	NP_543153.2:p.Gly519=