Canonical Allele Identifier: CA375740755

Gene: SLC34A3

Linked Data

• dbSNP Id: rs148095831
• gnomAD v3: 9-137236089-C-A
• gnomAD v4: 9-137236089-C-A
• MyVariant Identifiers: chr9:g.140130541C>A (hg19) ; chr9:g.137236089C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137236089C>A , CM000671.2:g.137236089C>A	GRCh38
NC_000009.11:g.140130541C>A , CM000671.1:g.140130541C>A	GRCh37
NC_000009.10:g.139250362C>A	NCBI36
NG_017008.1:g.10333C>A
NG_017008.2:g.10189C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673835.1:c.1473C>A MANE Select	ENSP00000501114.1:p.Tyr491Ter
ENST00000361134.2:c.1473C>A	ENSP00000355353.2:p.Tyr491Ter
ENST00000538474.5:c.1473C>A	ENSP00000442397.1:p.Tyr491Ter
NM_001177316.1:c.1473C>A	NP_001170787.1:p.Tyr491Ter
NM_001177317.1:c.1473C>A	NP_001170788.1:p.Tyr491Ter
NM_080877.2:c.1473C>A	NP_543153.1:p.Tyr491Ter
XM_017014291.1:c.*32C>A	XP_016869780.1:n.*32C>A
XM_017014292.1:c.1473C>A	XP_016869781.1:p.Tyr491Ter
NM_001177316.2:c.1473C>A MANE Select	NP_001170787.2:p.Tyr491Ter
NM_001177317.2:c.1473C>A	NP_001170788.2:p.Tyr491Ter
NM_080877.3:c.1473C>A	NP_543153.2:p.Tyr491Ter