Canonical Allele Identifier: CA1072523426
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756210863

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414443_1414444insGCCTGGAGGGTCAGGGCAGGGAAGGCACTGGGTGGGGGG , CM000667.2:g.1414443_1414444insGCCTGGAGGGTCAGGGCAGGGAAGGCACTGGGTGGGGGG GRCh38
NC_000005.9:g.1414558_1414559insGCCTGGAGGGTCAGGGCAGGGAAGGCACTGGGTGGGGGG , CM000667.1:g.1414558_1414559insGCCTGGAGGGTCAGGGCAGGGAAGGCACTGGGTGGGGGG GRCh37
NC_000005.8:g.1467558_1467559insGCCTGGAGGGTCAGGGCAGGGAAGGCACTGGGTGGGGGG NCBI36
NG_015885.1:g.36004_36005insCCTGCCCTGACCCTCCAGGCCCCCCCACCCAGTGCCTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+266_1156+267insCCTGCCCTGACCCTCCAGGCCCCCCCACCCAGTGCCTTC MANE Select ENSP00000270349.9:n.1156+266_1156+267insCCTGCCCTGACCCTCCAGGCC...
ENST00000270349.11:c.1156+266_1156+267insCCTGCCCTGACCCTCCAGGCCCCCCCACCCAGTGCCTTC ENSP00000270349.9:n.1156+266_1156+267insCCTGCCCTGACCCTCCAGGCC...
NM_001044.4:c.1156+266_1156+267insCCTGCCCTGACCCTCCAGGCCCCCCCACCCAGTGCCTTC NP_001035.1:n.1156+266_1156+267insCCTGCCCTGACCCTCCAGGCCCCCCCA...
NM_001044.5:c.1156+266_1156+267insCCTGCCCTGACCCTCCAGGCCCCCCCACCCAGTGCCTTC MANE Select NP_001035.1:n.1156+266_1156+267insCCTGCCCTGACCCTCCAGGCCCCCCCA...