Canonical Allele Identifier: CA1522627052
Gene: SLC6A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414453_1414491delinsGCAGGGCGGGGAAGGCGCTGGGTGGGGGGCCTGGAGGGT , CM000667.2:g.1414453_1414491delinsGCAGGGCGGGGAAGGCGCTGGGTGGGGGGCCTGGAGGGT GRCh38
NC_000005.9:g.1414568_1414606delinsGCAGGGCGGGGAAGGCGCTGGGTGGGGGGCCTGGAGGGT , CM000667.1:g.1414568_1414606delinsGCAGGGCGGGGAAGGCGCTGGGTGGGGGGCCTGGAGGGT GRCh37
NC_000005.8:g.1467568_1467606delinsGCAGGGCGGGGAAGGCGCTGGGTGGGGGGCCTGGAGGGT NCBI36
NG_015885.1:g.35938_35976delinsACCCTCCAGGCCCCCCACCCAGCGCCTTCCCCGCCCTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+200_1156+238delinsACCCTCCAGGCCCCCCACCCAGCGCCTTCCCCGCCCTGC MANE Select ENSP00000270349.9:n.1156+200_1156+238delinsACCCTCCAGGCCCCCCAC...
ENST00000270349.11:c.1156+200_1156+238delinsACCCTCCAGGCCCCCCACCCAGCGCCTTCCCCGCCCTGC ENSP00000270349.9:n.1156+200_1156+238delinsACCCTCCAGGCCCCCCAC...
NM_001044.4:c.1156+200_1156+238delinsACCCTCCAGGCCCCCCACCCAGCGCCTTCCCCGCCCTGC NP_001035.1:n.1156+200_1156+238delinsACCCTCCAGGCCCCCCACCCAGCG...
NM_001044.5:c.1156+200_1156+238delinsACCCTCCAGGCCCCCCACCCAGCGCCTTCCCCGCCCTGC MANE Select NP_001035.1:n.1156+200_1156+238delinsACCCTCCAGGCCCCCCACCCAGCG...