Canonical Allele Identifier: CA495567883
Gene: SLC6A2 HGNC NCBI

Linked Data

dbSNP Id: rs1286567467

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55699633C>T , CM000678.2:g.55699633C>T GRCh38
NC_000016.9:g.55733545C>T , CM000678.1:g.55733545C>T GRCh37
NC_000016.8:g.54291046C>T NCBI36
NG_016969.1:g.49004C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000219833.13:c.1569C>T ENSP00000219833.8:p.Phe523=
ENST00000568943.6:c.1569C>T MANE Select ENSP00000457473.1:p.Phe523=
ENST00000574918.2:c.1434C>T ENSP00000460214.2:p.Phe478=
ENST00000682050.1:c.*268C>T ENSP00000508367.1:n.*268C>T
ENST00000219833.12:c.1569C>T ENSP00000219833.8:p.Phe523=
ENST00000379906.6:c.1569C>T ENSP00000369237.2:p.Phe523=
ENST00000414754.7:c.1569C>T ENSP00000394956.3:p.Phe523=
ENST00000561820.5:c.1569C>T ENSP00000454439.1:p.Phe523=
ENST00000566163.5:c.1434C>T ENSP00000456210.1:p.Phe478=
ENST00000567238.1:c.1254C>T ENSP00000457375.1:p.Phe418=
ENST00000568943.5:c.1569C>T ENSP00000457473.1:p.Phe523=
NM_001043.3:c.1569C>T NP_001034.1:p.Phe523=
NM_001172501.1:c.1569C>T NP_001165972.1:p.Phe523=
NM_001172502.1:c.1254C>T NP_001165973.1:p.Phe418=
NM_001172504.1:c.1569C>T NP_001165975.1:p.Phe523=
XM_006721263.2:c.1569C>T XP_006721326.1:p.Phe523=
XM_011523295.1:c.1569C>T XP_011521597.1:p.Phe523=
XM_011523296.1:c.1434C>T XP_011521598.1:p.Phe478=
XM_011523297.1:c.1434C>T XP_011521599.1:p.Phe478=
XM_011523299.1:c.846C>T XP_011521601.1:p.Phe282=
XM_011523300.1:c.846C>T XP_011521602.1:p.Phe282=
XR_933403.1:n.2107-506C>T
XM_011523295.2:c.1569C>T XP_011521597.1:p.Phe523=
XM_011523296.2:c.1434C>T XP_011521598.1:p.Phe478=
XM_011523297.3:c.1434C>T XP_011521599.1:p.Phe478=
XM_011523299.2:c.846C>T XP_011521601.1:p.Phe282=
XM_011523300.2:c.846C>T XP_011521602.1:p.Phe282=
XR_933403.3:n.1783-506C>T
NM_001172501.2:c.1569C>T NP_001165972.1:p.Phe523=
NM_001172501.3:c.1569C>T MANE Select NP_001165972.1:p.Phe523=