Canonical Allele Identifier: CA112961834
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1374140427

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1411875_1411904dup , CM000667.2:g.1411875_1411904dup GRCh38
NC_000005.9:g.1411990_1412019dup , CM000667.1:g.1411990_1412019dup GRCh37
NC_000005.8:g.1464990_1465019dup NCBI36
NG_015885.1:g.38659_38688dup

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.1157-415_1157-386dup MANE Select ENSP00000270349.9:n.1157-415_1157-386dup
ENST00000270349.11:c.1157-415_1157-386dup ENSP00000270349.9:n.1157-415_1157-386dup
NM_001044.4:c.1157-415_1157-386dup NP_001035.1:n.1157-415_1157-386dup
NM_001044.5:c.1157-415_1157-386dup MANE Select NP_001035.1:n.1157-415_1157-386dup