Canonical Allele Identifier: CA2255095549
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1906886409

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30224995_30224996dup , CM000679.2:g.30224995_30224996dup GRCh38
NC_000017.10:g.28552013_28552014dup , CM000679.1:g.28552013_28552014dup GRCh37
NC_000017.9:g.25576139_25576140dup NCBI36
NG_011747.2:g.15941_15942dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.-220-2081_-220-2080dup MANE Select ENSP00000498537.1:n.-220-2081_-220-2080dup
ENST00000261707.7:c.-220-2081_-220-2080dup ENSP00000261707.3:n.-220-2081_-220-2080dup
ENST00000394821.2:c.-220-2081_-220-2080dup ENSP00000378298.2:n.-220-2081_-220-2080dup
ENST00000401766.6:c.-123-2915_-123-2914dup ENSP00000385822.2:n.-123-2915_-123-2914dup
NM_001045.5:c.-220-2081_-220-2080dup NP_001036.1:n.-220-2081_-220-2080dup
NM_001045.6:c.-220-2081_-220-2080dup MANE Select NP_001036.1:n.-220-2081_-220-2080dup