Canonical Allele Identifier: CA917398639
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1579709578

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414506_1414507insACTGGGTGGGGGGCCTGGAGGGTCAGGGCAGGGAAGGC , CM000667.2:g.1414506_1414507insACTGGGTGGGGGGCCTGGAGGGTCAGGGCAGGGAAGGC GRCh38
NC_000005.9:g.1414621_1414622insACTGGGTGGGGGGCCTGGAGGGTCAGGGCAGGGAAGGC , CM000667.1:g.1414621_1414622insACTGGGTGGGGGGCCTGGAGGGTCAGGGCAGGGAAGGC GRCh37
NC_000005.8:g.1467621_1467622insACTGGGTGGGGGGCCTGGAGGGTCAGGGCAGGGAAGGC NCBI36
NG_015885.1:g.35930_35931insTGCCCTGACCCTCCAGGCCCCCCACCCAGTGCCTTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+192_1156+193insTGCCCTGACCCTCCAGGCCCCCCACCCAGTGCCTTCCC MANE Select ENSP00000270349.9:n.1156+192_1156+193insTGCCCTGACCCTCCAGGCCCC...
ENST00000270349.11:c.1156+192_1156+193insTGCCCTGACCCTCCAGGCCCCCCACCCAGTGCCTTCCC ENSP00000270349.9:n.1156+192_1156+193insTGCCCTGACCCTCCAGGCCCC...
NM_001044.4:c.1156+192_1156+193insTGCCCTGACCCTCCAGGCCCCCCACCCAGTGCCTTCCC NP_001035.1:n.1156+192_1156+193insTGCCCTGACCCTCCAGGCCCCCCACCC...
NM_001044.5:c.1156+192_1156+193insTGCCCTGACCCTCCAGGCCCCCCACCCAGTGCCTTCCC MANE Select NP_001035.1:n.1156+192_1156+193insTGCCCTGACCCTCCAGGCCCCCCACCC...