Canonical Allele Identifier: CA804747808
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs892982329
gnomAD v3: 5-1410928-ATGTG-A
gnomAD v4: 5-1410928-ATGTG-A
MyVariant Identifiers: chr5:g.1411044_1411047del (hg19) chr5:g.1410929_1410932del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1410932_1410935del , CM000667.2:g.1410932_1410935del GRCh38
NC_000005.9:g.1411047_1411050del , CM000667.1:g.1411047_1411050del GRCh37
NC_000005.8:g.1464047_1464050del NCBI36
NG_015885.1:g.39497_39500del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1269+311_1269+314del MANE Select ENSP00000270349.9:n.1269+311_1269+314del
ENST00000270349.11:c.1269+311_1269+314del ENSP00000270349.9:n.1269+311_1269+314del
NM_001044.4:c.1269+311_1269+314del NP_001035.1:n.1269+311_1269+314del
NM_001044.5:c.1269+311_1269+314del MANE Select NP_001035.1:n.1269+311_1269+314del
Search 100 bp 5'
Search 100 bp 3'