Canonical Allele Identifier: CA2255094091
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1906761018

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30221579del , CM000679.2:g.30221579del GRCh38
NC_000017.10:g.28548597del , CM000679.1:g.28548597del GRCh37
NC_000017.9:g.25572723del NCBI36
NG_011747.2:g.19358del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.343+37del MANE Select ENSP00000498537.1:n.343+37del
ENST00000261707.7:c.343+37del ENSP00000261707.3:n.343+37del
ENST00000394821.2:c.343+37del ENSP00000378298.2:n.343+37del
ENST00000401766.6:c.343+37del ENSP00000385822.2:n.343+37del
NM_001045.5:c.343+37del NP_001036.1:n.343+37del
NM_001045.6:c.343+37del MANE Select NP_001036.1:n.343+37del