Canonical Allele Identifier: CA2255095402
Gene: SLC6A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30224610G= , CM000679.2:g.30224610G= GRCh38
NC_000017.10:g.28551628G= , CM000679.1:g.28551628G= GRCh37
NC_000017.9:g.25575754G= NCBI36
NG_011747.2:g.16327C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650711.1:c.-220-1695C= MANE Select ENSP00000498537.1:n.-220-1695C=
ENST00000261707.7:c.-220-1695C= ENSP00000261707.3:n.-220-1695C=
ENST00000394821.2:c.-220-1695C= ENSP00000378298.2:n.-220-1695C=
ENST00000401766.6:c.-123-2529C= ENSP00000385822.2:n.-123-2529C=
NM_001045.5:c.-220-1695C= NP_001036.1:n.-220-1695C=
NM_001045.6:c.-220-1695C= MANE Select NP_001036.1:n.-220-1695C=