Canonical Allele Identifier: CA363158143
Gene: SLC17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.25812950T>G , CM000668.2:g.25812950T>G GRCh38
NC_000006.11:g.25813178T>G , CM000668.1:g.25813178T>G GRCh37
NC_000006.10:g.25921157T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000244527.10:c.778A>C MANE Select ENSP00000244527.4:p.Lys260Gln
ENST00000244527.8:c.778A>C ENSP00000244527.4:p.Lys260Gln
ENST00000377886.6:c.*29A>C ENSP00000367118.2:n.*29A>C
ENST00000468082.1:c.735+145A>C ENSP00000420546.1:n.735+145A>C
ENST00000476801.5:c.778A>C ENSP00000420614.1:p.Lys260Gln
NM_005074.3:c.778A>C NP_005065.2:p.Lys260Gln
XM_011514818.1:c.778A>C XP_011513120.1:p.Lys260Gln
XM_011514819.1:c.691A>C XP_011513121.1:p.Lys231Gln
XM_011514820.1:c.735+145A>C XP_011513122.1:n.735+145A>C
XM_011514821.1:c.565A>C XP_011513123.1:p.Lys189Gln
XM_011514818.2:c.928A>C XP_011513120.2:p.Lys310Gln
XM_011514819.2:c.841A>C XP_011513121.2:p.Lys281Gln
XM_011514820.2:c.885+145A>C XP_011513122.2:n.885+145A>C
XM_011514821.2:c.565A>C XP_011513123.1:p.Lys189Gln
XM_017011199.1:c.928A>C XP_016866688.1:p.Lys310Gln
XM_017011200.1:c.928A>C XP_016866689.1:p.Lys310Gln
XM_017011201.2:c.928A>C XP_016866690.1:p.Lys310Gln
XM_017011202.1:c.844A>C XP_016866691.1:p.Lys282Gln
NM_005074.5:c.778A>C MANE Select NP_005065.2:p.Lys260Gln