Canonical Allele Identifier: CA1072523503
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756210962

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414445_1414446insTGGAGGGTCAGGGCGGGGAAGGCACTGGGTGGGGGGCC , CM000667.2:g.1414445_1414446insTGGAGGGTCAGGGCGGGGAAGGCACTGGGTGGGGGGCC GRCh38
NC_000005.9:g.1414560_1414561insTGGAGGGTCAGGGCGGGGAAGGCACTGGGTGGGGGGCC , CM000667.1:g.1414560_1414561insTGGAGGGTCAGGGCGGGGAAGGCACTGGGTGGGGGGCC GRCh37
NC_000005.8:g.1467560_1467561insTGGAGGGTCAGGGCGGGGAAGGCACTGGGTGGGGGGCC NCBI36
NG_015885.1:g.36004_36005insCCCGCCCTGACCCTCCAGGCCCCCCACCCAGTGCCTTC

Transcript Alleles

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