Canonical Allele Identifier: CA112963473
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs781002615
MyVariant Identifiers: chr5:g.1433399_1433400insCGTC (hg19) chr5:g.1433284_1433285insCGTC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1433285_1433288dup , CM000667.2:g.1433285_1433288dup GRCh38
NC_000005.9:g.1433400_1433403dup , CM000667.1:g.1433400_1433403dup GRCh37
NC_000005.8:g.1486400_1486403dup NCBI36
NG_015885.1:g.17141_17144dup

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.419-590_419-587dup MANE Select ENSP00000270349.9:n.419-590_419-587dup
ENST00000270349.11:c.419-590_419-587dup ENSP00000270349.9:n.419-590_419-587dup
NM_001044.4:c.419-590_419-587dup NP_001035.1:n.419-590_419-587dup
NM_001044.5:c.419-590_419-587dup MANE Select NP_001035.1:n.419-590_419-587dup
Search 100 bp 5'
Search 100 bp 3'