Canonical Allele Identifier: CA1072521915
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756204622

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414423_1414424insGGAAGGCACTGGGTGGGGGGGCCTGGAGGGGCAGGGCGG , CM000667.2:g.1414423_1414424insGGAAGGCACTGGGTGGGGGGGCCTGGAGGGGCAGGGCGG GRCh38
NC_000005.9:g.1414538_1414539insGGAAGGCACTGGGTGGGGGGGCCTGGAGGGGCAGGGCGG , CM000667.1:g.1414538_1414539insGGAAGGCACTGGGTGGGGGGGCCTGGAGGGGCAGGGCGG GRCh37
NC_000005.8:g.1467538_1467539insGGAAGGCACTGGGTGGGGGGGCCTGGAGGGGCAGGGCGG NCBI36
NG_015885.1:g.36042_36043insCCCCGCCCTGCCCCTCCAGGCCCCCCCACCCAGTGCCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+304_1156+305insCCCCGCCCTGCCCCTCCAGGCCCCCCCACCCAGTGCCTT MANE Select ENSP00000270349.9:n.1156+304_1156+305insCCCCGCCCTGCCCCTCCAGGC...
ENST00000270349.11:c.1156+304_1156+305insCCCCGCCCTGCCCCTCCAGGCCCCCCCACCCAGTGCCTT ENSP00000270349.9:n.1156+304_1156+305insCCCCGCCCTGCCCCTCCAGGC...
NM_001044.4:c.1156+304_1156+305insCCCCGCCCTGCCCCTCCAGGCCCCCCCACCCAGTGCCTT NP_001035.1:n.1156+304_1156+305insCCCCGCCCTGCCCCTCCAGGCCCCCCC...
NM_001044.5:c.1156+304_1156+305insCCCCGCCCTGCCCCTCCAGGCCCCCCCACCCAGTGCCTT MANE Select NP_001035.1:n.1156+304_1156+305insCCCCGCCCTGCCCCTCCAGGCCCCCCC...