Canonical Allele Identifier: CA1522628169
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756234834

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414653_1414674del , CM000667.2:g.1414653_1414674del GRCh38
NC_000005.9:g.1414768_1414789del , CM000667.1:g.1414768_1414789del GRCh37
NC_000005.8:g.1467768_1467789del NCBI36
NG_015885.1:g.35760_35781del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+22_1156+43del MANE Select ENSP00000270349.9:n.1156+22_1156+43del
ENST00000270349.11:c.1156+22_1156+43del ENSP00000270349.9:n.1156+22_1156+43del
NM_001044.4:c.1156+22_1156+43del NP_001035.1:n.1156+22_1156+43del
NM_001044.5:c.1156+22_1156+43del MANE Select NP_001035.1:n.1156+22_1156+43del