Canonical Allele Identifier: CA804997816
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1195331908
MyVariant Identifiers: chr5:g.1444556_1444561del (hg19) chr5:g.1444441_1444446del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1444452_1444457del , CM000667.2:g.1444452_1444457del GRCh38
NC_000005.9:g.1444567_1444572del , CM000667.1:g.1444567_1444572del GRCh37
NC_000005.8:g.1497567_1497572del NCBI36
NG_015885.1:g.5983_5988del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.-46+902_-46+907del MANE Select ENSP00000270349.9:n.-46+902_-46+907del
ENST00000270349.11:c.-46+902_-46+907del ENSP00000270349.9:n.-46+902_-46+907del
NM_001044.4:c.-46+902_-46+907del NP_001035.1:n.-46+902_-46+907del
NM_001044.5:c.-46+902_-46+907del MANE Select NP_001035.1:n.-46+902_-46+907del
Search 100 bp 5'
Search 100 bp 3'