Canonical Allele Identifier: CA804747811
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1324091135
MyVariant Identifiers: chr5:g.1411048_1411051del (hg19) chr5:g.1410933_1410936del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1410936_1410939del , CM000667.2:g.1410936_1410939del GRCh38
NC_000005.9:g.1411051_1411054del , CM000667.1:g.1411051_1411054del GRCh37
NC_000005.8:g.1464051_1464054del NCBI36
NG_015885.1:g.39493_39496del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1269+307_1269+310del MANE Select ENSP00000270349.9:n.1269+307_1269+310del
ENST00000270349.11:c.1269+307_1269+310del ENSP00000270349.9:n.1269+307_1269+310del
NM_001044.4:c.1269+307_1269+310del NP_001035.1:n.1269+307_1269+310del
NM_001044.5:c.1269+307_1269+310del MANE Select NP_001035.1:n.1269+307_1269+310del
Search 100 bp 5'
Search 100 bp 3'