Canonical Allele Identifier: CA557555676
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1553989586
gnomAD v2: 5-1443789-C-CA
MyVariant Identifiers: chr5:g.1443789_1443790insA (hg19) chr5:g.1443790_1443796delinsATTTTTTT (hg19) chr5:g.1443674_1443675insA (hg38) chr5:g.1443675_1443681delinsATTTTTTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1443674_1443675insA , CM000667.2:g.1443674_1443675insA GRCh38
NC_000005.9:g.1443789_1443790insA , CM000667.1:g.1443789_1443790insA GRCh37
NC_000005.8:g.1496789_1496790insA NCBI36
NG_015885.1:g.6754_6755insT

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.-45-433_-45-432insT MANE Select ENSP00000270349.9:n.-45-433_-45-432insT
ENST00000270349.11:c.-45-433_-45-432insT ENSP00000270349.9:n.-45-433_-45-432insT
NM_001044.4:c.-45-433_-45-432insT NP_001035.1:n.-45-433_-45-432insT
NM_001044.5:c.-45-433_-45-432insT MANE Select NP_001035.1:n.-45-433_-45-432insT
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