Canonical Allele Identifier: CA379913822
Community Standard Title: NM_004211.5(SLC6A5):c.769C>T (p.Gln257Ter)
Gene: SLC6A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20607096C>T , CM000673.2:g.20607096C>T GRCh38
NC_000011.9:g.20628642C>T , CM000673.1:g.20628642C>T GRCh37
NC_000011.8:g.20585218C>T NCBI36
NG_013086.1:g.12697C>T
NG_013086.2:g.12697C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004211.5:c.769C>T MANE Select NP_004202.4:p.Gln257Ter
ENST00000525748.6:c.769C>T MANE Select ENSP00000434364.2:p.Gln257Ter
NM_001318369.1:c.67C>T NP_001305298.1:p.Gln23Ter
NM_001318369.2:c.67C>T NP_001305298.1:p.Gln23Ter
NM_004211.3:c.769C>T NP_004202.2:p.Gln257Ter
NM_004211.4:c.769C>T NP_004202.3:p.Gln257Ter
ENST00000298923.11:c.*66C>T ENSP00000298923.7:n.*66C>T
ENST00000525748.5:c.769C>T ENSP00000434364.1:p.Gln257Ter
XM_005253225.1:c.67C>T XP_005253282.1:p.Gln23Ter
XM_011520473.1:c.769C>T XP_011518775.1:p.Gln257Ter
XM_017018544.2:c.67C>T XP_016874033.1:p.Gln23Ter
XM_017018545.2:c.-57+7421C>T XP_016874034.1:n.-57+7421C>T