Canonical Allele Identifier: CA2533434533
Gene: SLC6A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55656395_55656411del , CM000678.2:g.55656395_55656411del GRCh38
NC_000016.9:g.55690307_55690323del , CM000678.1:g.55690307_55690323del GRCh37
NC_000016.8:g.54247808_54247824del NCBI36
NG_016969.1:g.5766_5782del

Transcript Alleles

HGVS Amino-acid change
ENST00000219833.13:c.-300_-284del ENSP00000219833.8:n.-300_-284del
ENST00000568943.6:c.-52+226_-51-233del MANE Select ENSP00000457473.1:n.-52+226_-51-233del
ENST00000574918.2:c.-52+43_-52+59del ENSP00000460214.2:n.-52+43_-52+59del
ENST00000682050.1:c.-52+43_-52+59del ENSP00000508367.1:n.-52+43_-52+59del
ENST00000414754.7:c.-52+226_-51-233del ENSP00000394956.3:n.-52+226_-51-233del
ENST00000568529.6:c.-52+226_-51-233del ENSP00000456377.2:n.-52+226_-51-233del
ENST00000568655.5:c.-52+43_-52+59del ENSP00000454603.1:n.-52+43_-52+59del
ENST00000568943.5:c.-52+226_-51-233del ENSP00000457473.1:n.-52+226_-51-233del
NM_001172501.1:c.-52+226_-51-233del NP_001165972.1:n.-52+226_-51-233del
XM_006721263.2:c.-52+43_-52+59del XP_006721326.1:n.-52+43_-52+59del
XM_011523295.1:c.-52+226_-51-233del XP_011521597.1:n.-52+226_-51-233del
XM_011523296.1:c.-52+226_-51-233del XP_011521598.1:n.-52+226_-51-233del
XM_011523297.1:c.-52+226_-51-233del XP_011521599.1:n.-52+226_-51-233del
XM_011523298.1:c.-52+226_-51-233del XP_011521600.1:n.-52+226_-51-233del
XR_933403.1:n.566+226_567-233del
XM_011523295.2:c.-52+226_-51-233del XP_011521597.1:n.-52+226_-51-233del
XM_011523296.2:c.-52+226_-51-233del XP_011521598.1:n.-52+226_-51-233del
XM_011523297.3:c.-52+226_-51-233del XP_011521599.1:n.-52+226_-51-233del
XM_011523298.2:c.-52+226_-51-233del XP_011521600.1:n.-52+226_-51-233del
XR_933403.3:n.242+226_243-233del
NM_001172501.2:c.-52+226_-51-233del NP_001165972.1:n.-52+226_-51-233del
NM_001172501.3:c.-52+226_-51-233del MANE Select NP_001165972.1:n.-52+226_-51-233del