Canonical Allele Identifier: CA2255105447
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1906393175

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30211757dup , CM000679.2:g.30211757dup GRCh38
NC_000017.10:g.28538775dup , CM000679.1:g.28538775dup GRCh37
NC_000017.9:g.25562901dup NCBI36
NG_011747.2:g.29182dup

Transcript Alleles

HGVS Amino-acid change
ENST00000650711.1:c.1205-331dup MANE Select ENSP00000498537.1:n.1205-331dup
ENST00000261707.7:c.1205-331dup ENSP00000261707.3:n.1205-331dup
ENST00000394821.2:c.1205-331dup ENSP00000378298.2:n.1205-331dup
ENST00000401766.6:c.1205-331dup ENSP00000385822.2:n.1205-331dup
NM_001045.5:c.1205-331dup NP_001036.1:n.1205-331dup
NM_001045.6:c.1205-331dup MANE Select NP_001036.1:n.1205-331dup