Canonical Allele Identifier: CA557566096
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1560913099
gnomAD v2: 5-1414631-G-GGGGCCTGGAGGGGCAGGGCGGGGAA
gnomAD v3: 5-1414516-G-GGGGCCTGGAGGGGCAGGGCGGGGAA
gnomAD v4: 5-1414516-G-GGGGCCTGGAGGGGCAGGGCGGGGAA
MyVariant Identifiers: chr5:g.1414631_1414632insGGGCCTGGAGGGGCAGGGCGGGGAA (hg19) chr5:g.1414516_1414517insGGGCCTGGAGGGGCAGGGCGGGGAA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414518_1414519insGCCTGGAGGGGCAGGGCGGGGAAGG , CM000667.2:g.1414518_1414519insGCCTGGAGGGGCAGGGCGGGGAAGG GRCh38
NC_000005.9:g.1414633_1414634insGCCTGGAGGGGCAGGGCGGGGAAGG , CM000667.1:g.1414633_1414634insGCCTGGAGGGGCAGGGCGGGGAAGG GRCh37
NC_000005.8:g.1467633_1467634insGCCTGGAGGGGCAGGGCGGGGAAGG NCBI36
NG_015885.1:g.35912_35913insTTCCCCGCCCTGCCCCTCCAGGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+174_1156+175insTTCCCCGCCCTGCCCCTCCAGGCCC MANE Select ENSP00000270349.9:n.1156+174_1156+175insTTCCCCGCCCTGCCCCTCCAG...
ENST00000270349.11:c.1156+174_1156+175insTTCCCCGCCCTGCCCCTCCAGGCCC ENSP00000270349.9:n.1156+174_1156+175insTTCCCCGCCCTGCCCCTCCAG...
NM_001044.4:c.1156+174_1156+175insTTCCCCGCCCTGCCCCTCCAGGCCC NP_001035.1:n.1156+174_1156+175insTTCCCCGCCCTGCCCCTCCAGGCCC
NM_001044.5:c.1156+174_1156+175insTTCCCCGCCCTGCCCCTCCAGGCCC MANE Select NP_001035.1:n.1156+174_1156+175insTTCCCCGCCCTGCCCCTCCAGGCCC
Search 100 bp 5'
Search 100 bp 3'