Canonical Allele Identifier: CA919823812
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1567822682

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30224899_30224905del , CM000679.2:g.30224899_30224905del GRCh38
NC_000017.10:g.28551917_28551923del , CM000679.1:g.28551917_28551923del GRCh37
NC_000017.9:g.25576043_25576049del NCBI36
NG_011747.2:g.16034_16040del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.-220-1988_-220-1982del MANE Select ENSP00000498537.1:n.-220-1988_-220-1982del
ENST00000261707.7:c.-220-1988_-220-1982del ENSP00000261707.3:n.-220-1988_-220-1982del
ENST00000394821.2:c.-220-1988_-220-1982del ENSP00000378298.2:n.-220-1988_-220-1982del
ENST00000401766.6:c.-123-2822_-123-2816del ENSP00000385822.2:n.-123-2822_-123-2816del
NM_001045.5:c.-220-1988_-220-1982del NP_001036.1:n.-220-1988_-220-1982del
NM_001045.6:c.-220-1988_-220-1982del MANE Select NP_001036.1:n.-220-1988_-220-1982del