Canonical Allele Identifier: CA364718111

Gene: SLC17A5

Linked Data

• dbSNP Id: rs779264733
• gnomAD v3: 6-73641795-A-C
• gnomAD v4: 6-73641795-A-C
• MyVariant Identifiers: chr6:g.74351518A>C (hg19) ; chr6:g.73641795A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73641795A>C , CM000668.2:g.73641795A>C	GRCh38
NC_000006.11:g.74351518A>C , CM000668.1:g.74351518A>C	GRCh37
NC_000006.10:g.74408239A>C	NCBI36
NG_008272.1:g.17220T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.421T>G MANE Select	ENSP00000348019.5:p.Phe141Val
ENST00000355773.5:c.421T>G	ENSP00000348019.5:p.Phe141Val
ENST00000481996.1:n.187T>G
NM_012434.4:c.421T>G	NP_036566.1:p.Phe141Val
XM_005248710.2:c.370T>G	XP_005248767.1:p.Phe124Val
XM_005248711.1:c.223T>G	XP_005248768.1:p.Phe75Val
XM_011535750.1:c.421T>G	XP_011534052.1:p.Phe141Val
XM_011535751.1:c.421T>G	XP_011534053.1:p.Phe141Val
NM_012434.5:c.421T>G MANE Select	NP_036566.1:p.Phe141Val
NM_001382629.1:c.190T>G	NP_001369558.1:p.Phe64Val
NM_001382630.1:c.421T>G	NP_001369559.1:p.Phe141Val
NM_001382631.1:c.442T>G	NP_001369560.1:p.Phe148Val
NM_001382632.1:c.421T>G	NP_001369561.1:p.Phe141Val
NM_001382633.1:c.421T>G	NP_001369562.1:p.Phe141Val
NM_001382634.1:c.421T>G	NP_001369563.1:p.Phe141Val
NM_001382635.1:c.421T>G	NP_001369564.1:p.Phe141Val
NM_001382636.1:c.190T>G	NP_001369565.1:p.Phe64Val