Canonical Allele Identifier: CA721928074
Gene: SLC6A2 HGNC NCBI

Linked Data

dbSNP Id: rs1247124088

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55656482_55656483del , CM000678.2:g.55656482_55656483del GRCh38
NC_000016.9:g.55690394_55690395del , CM000678.1:g.55690394_55690395del GRCh37
NC_000016.8:g.54247895_54247896del NCBI36
NG_016969.1:g.5853_5854del

Transcript Alleles

HGVS Amino-acid change
ENST00000219833.13:c.-213_-212del ENSP00000219833.8:n.-213_-212del
ENST00000568943.6:c.-51-162_-51-161del MANE Select ENSP00000457473.1:n.-51-162_-51-161del
ENST00000574918.2:c.-52+130_-52+131del ENSP00000460214.2:n.-52+130_-52+131del
ENST00000682050.1:c.-52+130_-52+131del ENSP00000508367.1:n.-52+130_-52+131del
ENST00000379906.6:c.-213_-212del ENSP00000369237.2:n.-213_-212del
ENST00000414754.7:c.-51-162_-51-161del ENSP00000394956.3:n.-51-162_-51-161del
ENST00000568529.6:c.-51-162_-51-161del ENSP00000456377.2:n.-51-162_-51-161del
ENST00000568655.5:c.-52+130_-52+131del ENSP00000454603.1:n.-52+130_-52+131del
ENST00000568943.5:c.-51-162_-51-161del ENSP00000457473.1:n.-51-162_-51-161del
NM_001043.3:c.-213_-212del NP_001034.1:n.-213_-212del
NM_001172501.1:c.-51-162_-51-161del NP_001165972.1:n.-51-162_-51-161del
XM_006721263.2:c.-52+130_-52+131del XP_006721326.1:n.-52+130_-52+131del
XM_011523295.1:c.-51-162_-51-161del XP_011521597.1:n.-51-162_-51-161del
XM_011523296.1:c.-51-162_-51-161del XP_011521598.1:n.-51-162_-51-161del
XM_011523297.1:c.-51-162_-51-161del XP_011521599.1:n.-51-162_-51-161del
XM_011523298.1:c.-51-162_-51-161del XP_011521600.1:n.-51-162_-51-161del
XR_933403.1:n.567-162_567-161del
XM_011523295.2:c.-51-162_-51-161del XP_011521597.1:n.-51-162_-51-161del
XM_011523296.2:c.-51-162_-51-161del XP_011521598.1:n.-51-162_-51-161del
XM_011523297.3:c.-51-162_-51-161del XP_011521599.1:n.-51-162_-51-161del
XM_011523298.2:c.-51-162_-51-161del XP_011521600.1:n.-51-162_-51-161del
XR_933403.3:n.243-162_243-161del
NM_001172501.2:c.-51-162_-51-161del NP_001165972.1:n.-51-162_-51-161del
NM_001172501.3:c.-51-162_-51-161del MANE Select NP_001165972.1:n.-51-162_-51-161del