Canonical Allele Identifier: CA1072526546
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756222071

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414506_1414507insACTGGGTGGGGGGCCTGGAGGGGCAGGGCGGGGAAGGC , CM000667.2:g.1414506_1414507insACTGGGTGGGGGGCCTGGAGGGGCAGGGCGGGGAAGGC GRCh38
NC_000005.9:g.1414621_1414622insACTGGGTGGGGGGCCTGGAGGGGCAGGGCGGGGAAGGC , CM000667.1:g.1414621_1414622insACTGGGTGGGGGGCCTGGAGGGGCAGGGCGGGGAAGGC GRCh37
NC_000005.8:g.1467621_1467622insACTGGGTGGGGGGCCTGGAGGGGCAGGGCGGGGAAGGC NCBI36
NG_015885.1:g.35937_35938insCCCCTCCAGGCCCCCCACCCAGTGCCTTCCCCGCCCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+199_1156+200insCCCCTCCAGGCCCCCCACCCAGTGCCTTCCCCGCCCTG MANE Select ENSP00000270349.9:n.1156+199_1156+200insCCCCTCCAGGCCCCCCACCCA...
ENST00000270349.11:c.1156+199_1156+200insCCCCTCCAGGCCCCCCACCCAGTGCCTTCCCCGCCCTG ENSP00000270349.9:n.1156+199_1156+200insCCCCTCCAGGCCCCCCACCCA...
NM_001044.4:c.1156+199_1156+200insCCCCTCCAGGCCCCCCACCCAGTGCCTTCCCCGCCCTG NP_001035.1:n.1156+199_1156+200insCCCCTCCAGGCCCCCCACCCAGTGCCT...
NM_001044.5:c.1156+199_1156+200insCCCCTCCAGGCCCCCCACCCAGTGCCTTCCCCGCCCTG MANE Select NP_001035.1:n.1156+199_1156+200insCCCCTCCAGGCCCCCCACCCAGTGCCT...