Canonical Allele Identifier: CA1522626541
Gene: SLC6A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414369_1414408delinsGAGAGGCACAAGGCAGGAAAGGCACTGGGTGGGGGGGCCT , CM000667.2:g.1414369_1414408delinsGAGAGGCACAAGGCAGGAAAGGCACTGGGTGGGGGGGCCT GRCh38
NC_000005.9:g.1414484_1414523delinsGAGAGGCACAAGGCAGGAAAGGCACTGGGTGGGGGGGCCT , CM000667.1:g.1414484_1414523delinsGAGAGGCACAAGGCAGGAAAGGCACTGGGTGGGGGGGCCT GRCh37
NC_000005.8:g.1467484_1467523delinsGAGAGGCACAAGGCAGGAAAGGCACTGGGTGGGGGGGCCT NCBI36
NG_015885.1:g.36021_36060delinsAGGCCCCCCCACCCAGTGCCTTTCCTGCCTTGTGCCTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+283_1156+322delinsAGGCCCCCCCACCCAGTGCCTTTCCTGCCTTGTGCCTCTC MANE Select ENSP00000270349.9:n.1156+283_1156+322delinsAGGCCCCCCCACCCAGTG...
ENST00000270349.11:c.1156+283_1156+322delinsAGGCCCCCCCACCCAGTGCCTTTCCTGCCTTGTGCCTCTC ENSP00000270349.9:n.1156+283_1156+322delinsAGGCCCCCCCACCCAGTG...
NM_001044.4:c.1156+283_1156+322delinsAGGCCCCCCCACCCAGTGCCTTTCCTGCCTTGTGCCTCTC NP_001035.1:n.1156+283_1156+322delinsAGGCCCCCCCACCCAGTGCCTTTC...
NM_001044.5:c.1156+283_1156+322delinsAGGCCCCCCCACCCAGTGCCTTTCCTGCCTTGTGCCTCTC MANE Select NP_001035.1:n.1156+283_1156+322delinsAGGCCCCCCCACCCAGTGCCTTTC...