Canonical Allele Identifier: CA136234919
Gene: SLC17A1 HGNC NCBI

Linked Data

dbSNP Id: rs17342717
gnomAD v2: 6-25821770-C-T
gnomAD v3: 6-25821542-C-T
gnomAD v4: 6-25821542-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.25821542C>T , CM000668.2:g.25821542C>T GRCh38
NC_000006.11:g.25821770C>T , CM000668.1:g.25821770C>T GRCh37
NC_000006.10:g.25929749C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244527.10:c.208-1627G>A MANE Select ENSP00000244527.4:n.208-1627G>A
ENST00000244527.8:c.208-1627G>A ENSP00000244527.4:n.208-1627G>A
ENST00000377886.6:c.208-1627G>A ENSP00000367118.2:n.208-1627G>A
ENST00000468082.1:c.208-1627G>A ENSP00000420546.1:n.208-1627G>A
ENST00000476801.5:c.208-1627G>A ENSP00000420614.1:n.208-1627G>A
NM_005074.3:c.208-1627G>A NP_005065.2:n.208-1627G>A
XM_011514818.1:c.208-1627G>A XP_011513120.1:n.208-1627G>A
XM_011514819.1:c.208-1627G>A XP_011513121.1:n.208-1627G>A
XM_011514820.1:c.208-1627G>A XP_011513122.1:n.208-1627G>A
XM_011514821.1:c.-6-1627G>A XP_011513123.1:n.-6-1627G>A
XM_011514818.2:c.358-1627G>A XP_011513120.2:n.358-1627G>A
XM_011514819.2:c.358-1627G>A XP_011513121.2:n.358-1627G>A
XM_011514820.2:c.358-1627G>A XP_011513122.2:n.358-1627G>A
XM_011514821.2:c.-6-1627G>A XP_011513123.1:n.-6-1627G>A
XM_017011199.1:c.358-1627G>A XP_016866688.1:n.358-1627G>A
XM_017011200.1:c.358-1627G>A XP_016866689.1:n.358-1627G>A
XM_017011201.2:c.358-1627G>A XP_016866690.1:n.358-1627G>A
XM_017011202.1:c.274-1627G>A XP_016866691.1:n.274-1627G>A
NM_005074.5:c.208-1627G>A MANE Select NP_005065.2:n.208-1627G>A