Canonical Allele Identifier: CA2255095529
Gene: SLC6A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30224947_30224948delinsTG , CM000679.2:g.30224947_30224948delinsTG GRCh38
NC_000017.10:g.28551965_28551966delinsTG , CM000679.1:g.28551965_28551966delinsTG GRCh37
NC_000017.9:g.25576091_25576092delinsTG NCBI36
NG_011747.2:g.15989_15990delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.-220-2033_-220-2032delinsCA MANE Select ENSP00000498537.1:n.-220-2033_-220-2032delinsCA
ENST00000261707.7:c.-220-2033_-220-2032delinsCA ENSP00000261707.3:n.-220-2033_-220-2032delinsCA
ENST00000394821.2:c.-220-2033_-220-2032delinsCA ENSP00000378298.2:n.-220-2033_-220-2032delinsCA
ENST00000401766.6:c.-123-2867_-123-2866delinsCA ENSP00000385822.2:n.-123-2867_-123-2866delinsCA
NM_001045.5:c.-220-2033_-220-2032delinsCA NP_001036.1:n.-220-2033_-220-2032delinsCA
NM_001045.6:c.-220-2033_-220-2032delinsCA MANE Select NP_001036.1:n.-220-2033_-220-2032delinsCA