Canonical Allele Identifier: CA363157846
Gene: SLC17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.25812864A>C , CM000668.2:g.25812864A>C GRCh38
NC_000006.11:g.25813092A>C , CM000668.1:g.25813092A>C GRCh37
NC_000006.10:g.25921071A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000244527.10:c.864T>G MANE Select ENSP00000244527.4:p.Phe288Leu
ENST00000244527.8:c.864T>G ENSP00000244527.4:p.Phe288Leu
ENST00000377886.6:c.*115T>G ENSP00000367118.2:n.*115T>G
ENST00000468082.1:c.735+231T>G ENSP00000420546.1:n.735+231T>G
ENST00000476801.5:c.864T>G ENSP00000420614.1:p.Phe288Leu
NM_005074.3:c.864T>G NP_005065.2:p.Phe288Leu
XM_011514818.1:c.864T>G XP_011513120.1:p.Phe288Leu
XM_011514819.1:c.777T>G XP_011513121.1:p.Phe259Leu
XM_011514820.1:c.735+231T>G XP_011513122.1:n.735+231T>G
XM_011514821.1:c.651T>G XP_011513123.1:p.Phe217Leu
XM_011514818.2:c.1014T>G XP_011513120.2:p.Phe338Leu
XM_011514819.2:c.927T>G XP_011513121.2:p.Phe309Leu
XM_011514820.2:c.885+231T>G XP_011513122.2:n.885+231T>G
XM_011514821.2:c.651T>G XP_011513123.1:p.Phe217Leu
XM_017011199.1:c.1014T>G XP_016866688.1:p.Phe338Leu
XM_017011200.1:c.1014T>G XP_016866689.1:p.Phe338Leu
XM_017011201.2:c.1014T>G XP_016866690.1:p.Phe338Leu
XM_017011202.1:c.930T>G XP_016866691.1:p.Phe310Leu
NM_005074.5:c.864T>G MANE Select NP_005065.2:p.Phe288Leu