Canonical Allele Identifier: CA982856661
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1906753326

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30221478dup , CM000679.2:g.30221478dup GRCh38
NC_000017.10:g.28548496dup , CM000679.1:g.28548496dup GRCh37
NC_000017.9:g.25572622dup NCBI36
NG_011747.2:g.19461dup

Transcript Alleles

HGVS Amino-acid change
ENST00000650711.1:c.343+140dup MANE Select ENSP00000498537.1:n.343+140dup
ENST00000261707.7:c.343+140dup ENSP00000261707.3:n.343+140dup
ENST00000394821.2:c.343+140dup ENSP00000378298.2:n.343+140dup
ENST00000401766.6:c.343+140dup ENSP00000385822.2:n.343+140dup
NM_001045.5:c.343+140dup NP_001036.1:n.343+140dup
NM_001045.6:c.343+140dup MANE Select NP_001036.1:n.343+140dup