Canonical Allele Identifier: CA804747814

Gene: SLC6A3

Linked Data

• dbSNP Id: rs1390926226
• MyVariant Identifiers: chr5:g.1411053_1411060del (hg19) ; chr5:g.1410938_1410945del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1410942_1410949del , CM000667.2:g.1410942_1410949del	GRCh38
NC_000005.9:g.1411057_1411064del , CM000667.1:g.1411057_1411064del	GRCh37
NC_000005.8:g.1464057_1464064del	NCBI36
NG_015885.1:g.39484_39491del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270349.12:c.1269+298_1269+305del MANE Select	ENSP00000270349.9:n.1269+298_1269+305del
ENST00000270349.11:c.1269+298_1269+305del	ENSP00000270349.9:n.1269+298_1269+305del
NM_001044.4:c.1269+298_1269+305del	NP_001035.1:n.1269+298_1269+305del
NM_001044.5:c.1269+298_1269+305del MANE Select	NP_001035.1:n.1269+298_1269+305del