Canonical Allele Identifier: CA1072522625
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756207849

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414423_1414424insGGAAGGCACTGGGTGGGGGGCCGGGAGGGGCAGGGCGG , CM000667.2:g.1414423_1414424insGGAAGGCACTGGGTGGGGGGCCGGGAGGGGCAGGGCGG GRCh38
NC_000005.9:g.1414538_1414539insGGAAGGCACTGGGTGGGGGGCCGGGAGGGGCAGGGCGG , CM000667.1:g.1414538_1414539insGGAAGGCACTGGGTGGGGGGCCGGGAGGGGCAGGGCGG GRCh37
NC_000005.8:g.1467538_1467539insGGAAGGCACTGGGTGGGGGGCCGGGAGGGGCAGGGCGG NCBI36
NG_015885.1:g.36020_36021insCGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+282_1156+283insCGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCC MANE Select ENSP00000270349.9:n.1156+282_1156+283insCGGCCCCCCACCCAGTGCCTT...
ENST00000270349.11:c.1156+282_1156+283insCGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCC ENSP00000270349.9:n.1156+282_1156+283insCGGCCCCCCACCCAGTGCCTT...
NM_001044.4:c.1156+282_1156+283insCGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCC NP_001035.1:n.1156+282_1156+283insCGGCCCCCCACCCAGTGCCTTCCCCGC...
NM_001044.5:c.1156+282_1156+283insCGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCC MANE Select NP_001035.1:n.1156+282_1156+283insCGGCCCCCCACCCAGTGCCTTCCCCGC...