Canonical Allele Identifier: CA2223789932
Gene: SLC6A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55656440G= , CM000678.2:g.55656440G= GRCh38
NC_000016.9:g.55690352G= , CM000678.1:g.55690352G= GRCh37
NC_000016.8:g.54247853G= NCBI36
NG_016969.1:g.5811G=

Transcript Alleles

HGVS Amino-acid change
ENST00000219833.13:c.-255G= ENSP00000219833.8:n.-255G=
ENST00000568943.6:c.-51-204G= MANE Select ENSP00000457473.1:n.-51-204G=
ENST00000574918.2:c.-52+88G= ENSP00000460214.2:n.-52+88G=
ENST00000682050.1:c.-52+88G= ENSP00000508367.1:n.-52+88G=
ENST00000379906.6:c.-255G= ENSP00000369237.2:n.-255G=
ENST00000414754.7:c.-51-204G= ENSP00000394956.3:n.-51-204G=
ENST00000568529.6:c.-51-204G= ENSP00000456377.2:n.-51-204G=
ENST00000568655.5:c.-52+88G= ENSP00000454603.1:n.-52+88G=
ENST00000568943.5:c.-51-204G= ENSP00000457473.1:n.-51-204G=
NM_001043.3:c.-255G= NP_001034.1:n.-255G=
NM_001172501.1:c.-51-204G= NP_001165972.1:n.-51-204G=
XM_006721263.2:c.-52+88G= XP_006721326.1:n.-52+88G=
XM_011523295.1:c.-51-204G= XP_011521597.1:n.-51-204G=
XM_011523296.1:c.-51-204G= XP_011521598.1:n.-51-204G=
XM_011523297.1:c.-51-204G= XP_011521599.1:n.-51-204G=
XM_011523298.1:c.-51-204G= XP_011521600.1:n.-51-204G=
XR_933403.1:n.567-204G=
XM_011523295.2:c.-51-204G= XP_011521597.1:n.-51-204G=
XM_011523296.2:c.-51-204G= XP_011521598.1:n.-51-204G=
XM_011523297.3:c.-51-204G= XP_011521599.1:n.-51-204G=
XM_011523298.2:c.-51-204G= XP_011521600.1:n.-51-204G=
XR_933403.3:n.243-204G=
NM_001172501.2:c.-51-204G= NP_001165972.1:n.-51-204G=
NM_001172501.3:c.-51-204G= MANE Select NP_001165972.1:n.-51-204G=