Canonical Allele Identifier: CA1956624655
Gene: SLC6A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20638433T= , CM000673.2:g.20638433T= GRCh38
NC_000011.9:g.20659979T= , CM000673.1:g.20659979T= GRCh37
NC_000011.8:g.20616555T= NCBI36
NG_013086.1:g.44034T=
NG_013086.2:g.44034T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525748.6:c.1870-26T= MANE Select ENSP00000434364.2:n.1870-26T=
ENST00000298923.11:c.*1167-26T= ENSP00000298923.7:n.*1167-26T=
ENST00000525748.5:c.1870-26T= ENSP00000434364.1:n.1870-26T=
ENST00000528440.1:n.401-26T=
NM_004211.3:c.1870-26T= NP_004202.2:n.1870-26T=
XM_005253225.1:c.1168-26T= XP_005253282.1:n.1168-26T=
XM_011520473.1:c.1870-26T= XP_011518775.1:n.1870-26T=
NM_001318369.1:c.1168-26T= NP_001305298.1:n.1168-26T=
NM_004211.4:c.1870-26T= NP_004202.3:n.1870-26T=
XM_017018544.2:c.994-26T= XP_016874033.1:n.994-26T=
XM_017018545.2:c.829-26T= XP_016874034.1:n.829-26T=
NM_001318369.2:c.1168-26T= NP_001305298.1:n.1168-26T=
NM_004211.5:c.1870-26T= MANE Select NP_004202.4:n.1870-26T=