Canonical Allele Identifier: CA375730988

Gene: SLC34A3

Linked Data

• dbSNP Id: rs121918237
• gnomAD v2: 9-140127686-G-T
• gnomAD v4: 9-137233234-G-T
• MyVariant Identifiers: chr9:g.140127686G>T (hg19) ; chr9:g.137233234G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137233234G>T , CM000671.2:g.137233234G>T	GRCh38
NC_000009.11:g.140127686G>T , CM000671.1:g.140127686G>T	GRCh37
NC_000009.10:g.139247507G>T	NCBI36
NG_017008.1:g.7478G>T
NG_017008.2:g.7334G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000673835.1:c.586G>T MANE Select	ENSP00000501114.1:p.Gly196Trp
ENST00000673865.1:c.586G>T	ENSP00000501101.1:p.Gly196Trp
ENST00000361134.2:c.586G>T	ENSP00000355353.2:p.Gly196Trp
ENST00000538474.5:c.586G>T	ENSP00000442397.1:p.Gly196Trp
NM_001177316.1:c.586G>T	NP_001170787.1:p.Gly196Trp
NM_001177317.1:c.586G>T	NP_001170788.1:p.Gly196Trp
NM_080877.2:c.586G>T	NP_543153.1:p.Gly196Trp
XM_011518256.1:c.586G>T	XP_011516558.1:p.Gly196Trp
XM_011518257.1:c.586G>T	XP_011516559.1:p.Gly196Trp
XM_011518258.1:c.586G>T	XP_011516560.1:p.Gly196Trp
XM_011518259.1:c.586G>T	XP_011516561.1:p.Gly196Trp
XM_011518260.1:c.586G>T	XP_011516562.1:p.Gly196Trp
XM_011518261.1:c.586G>T	XP_011516563.1:p.Gly196Trp
XM_011518262.1:c.586G>T	XP_011516564.1:p.Gly196Trp
XM_011518257.2:c.586G>T	XP_011516559.1:p.Gly196Trp
XM_011518261.2:c.586G>T	XP_011516563.1:p.Gly196Trp
XM_017014290.1:c.586G>T	XP_016869779.1:p.Gly196Trp
XM_017014291.1:c.586G>T	XP_016869780.1:p.Gly196Trp
XM_017014292.1:c.586G>T	XP_016869781.1:p.Gly196Trp
NM_001177316.2:c.586G>T MANE Select	NP_001170787.2:p.Gly196Trp
NM_001177317.2:c.586G>T	NP_001170788.2:p.Gly196Trp
NM_080877.3:c.586G>T	NP_543153.2:p.Gly196Trp