Canonical Allele Identifier: CA1522627088
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756215283

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414461_1414463del , CM000667.2:g.1414461_1414463del GRCh38
NC_000005.9:g.1414576_1414578del , CM000667.1:g.1414576_1414578del GRCh37
NC_000005.8:g.1467576_1467578del NCBI36
NG_015885.1:g.35967_35969del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+229_1156+231del MANE Select ENSP00000270349.9:n.1156+229_1156+231del
ENST00000270349.11:c.1156+229_1156+231del ENSP00000270349.9:n.1156+229_1156+231del
NM_001044.4:c.1156+229_1156+231del NP_001035.1:n.1156+229_1156+231del
NM_001044.5:c.1156+229_1156+231del MANE Select NP_001035.1:n.1156+229_1156+231del