Canonical Allele Identifier: CA5921786
Community Standard Title: NM_004211.5(SLC6A5):c.*3C>T
Gene: SLC6A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20654871C>T , CM000673.2:g.20654871C>T GRCh38
NC_000011.9:g.20676417C>T , CM000673.1:g.20676417C>T GRCh37
NC_000011.8:g.20632993C>T NCBI36
NG_013086.1:g.60472C>T
NG_013086.2:g.60472C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004211.5:c.*3C>T MANE Select NP_004202.4:n.*3C>T
ENST00000525748.6:c.*3C>T MANE Select ENSP00000434364.2:n.*3C>T
NM_001318369.1:c.*3C>T NP_001305298.1:n.*3C>T
NM_001318369.2:c.*3C>T NP_001305298.1:n.*3C>T
NM_004211.3:c.*3C>T NP_004202.2:n.*3C>T
NM_004211.4:c.*3C>T NP_004202.3:n.*3C>T
ENST00000298923.11:c.*1694C>T ENSP00000298923.7:n.*1694C>T
ENST00000525748.5:c.*3C>T ENSP00000434364.1:n.*3C>T
ENST00000528440.1:n.928C>T
XM_005253225.1:c.*3C>T XP_005253282.1:n.*3C>T
XM_011520473.1:c.*3C>T XP_011518775.1:n.*3C>T
XM_017018544.2:c.*3C>T XP_016874033.1:n.*3C>T
XM_017018545.2:c.*3C>T XP_016874034.1:n.*3C>T