Canonical Allele Identifier: CA557566023
Gene: SLC6A3 HGNC NCBI

Linked Data

gnomAD v2: 5-1414557-GGCCGGGAGGGGCAGGGCGGGGAAGGC-G
MyVariant Identifiers: chr5:g.1414558_1414583del (hg19) chr5:g.1414443_1414468del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414445_1414470del , CM000667.2:g.1414445_1414470del GRCh38
NC_000005.9:g.1414560_1414585del , CM000667.1:g.1414560_1414585del GRCh37
NC_000005.8:g.1467560_1467585del NCBI36
NG_015885.1:g.35961_35986del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+223_1156+248del MANE Select ENSP00000270349.9:n.1156+223_1156+248del
ENST00000270349.11:c.1156+223_1156+248del ENSP00000270349.9:n.1156+223_1156+248del
NM_001044.4:c.1156+223_1156+248del NP_001035.1:n.1156+223_1156+248del
NM_001044.5:c.1156+223_1156+248del MANE Select NP_001035.1:n.1156+223_1156+248del
Search 100 bp 5'
Search 100 bp 3'