Canonical Allele Identifier: CA2255094074
Gene: SLC6A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30221559_30221560delinsCT , CM000679.2:g.30221559_30221560delinsCT GRCh38
NC_000017.10:g.28548577_28548578delinsCT , CM000679.1:g.28548577_28548578delinsCT GRCh37
NC_000017.9:g.25572703_25572704delinsCT NCBI36
NG_011747.2:g.19377_19378delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.343+56_343+57delinsAG MANE Select ENSP00000498537.1:n.343+56_343+57delinsAG
ENST00000261707.7:c.343+56_343+57delinsAG ENSP00000261707.3:n.343+56_343+57delinsAG
ENST00000394821.2:c.343+56_343+57delinsAG ENSP00000378298.2:n.343+56_343+57delinsAG
ENST00000401766.6:c.343+56_343+57delinsAG ENSP00000385822.2:n.343+56_343+57delinsAG
NM_001045.5:c.343+56_343+57delinsAG NP_001036.1:n.343+56_343+57delinsAG
NM_001045.6:c.343+56_343+57delinsAG MANE Select NP_001036.1:n.343+56_343+57delinsAG