Canonical Allele Identifier: CA804747826
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1181664880
gnomAD v3: 5-1410949-TATGTGTGTGTGTGC-T
gnomAD v4: 5-1410949-TATGTGTGTGTGTGC-T
MyVariant Identifiers: chr5:g.1411065_1411078del (hg19) chr5:g.1410950_1410963del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1410959_1410972del , CM000667.2:g.1410959_1410972del GRCh38
NC_000005.9:g.1411074_1411087del , CM000667.1:g.1411074_1411087del GRCh37
NC_000005.8:g.1464074_1464087del NCBI36
NG_015885.1:g.39466_39479del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1269+280_1269+293del MANE Select ENSP00000270349.9:n.1269+280_1269+293del
ENST00000270349.11:c.1269+280_1269+293del ENSP00000270349.9:n.1269+280_1269+293del
NM_001044.4:c.1269+280_1269+293del NP_001035.1:n.1269+280_1269+293del
NM_001044.5:c.1269+280_1269+293del MANE Select NP_001035.1:n.1269+280_1269+293del
Search 100 bp 5'
Search 100 bp 3'