Canonical Allele Identifier: CA1956619747
Gene: SLC6A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20628026C= , CM000673.2:g.20628026C= GRCh38
NC_000011.9:g.20649572C= , CM000673.1:g.20649572C= GRCh37
NC_000011.8:g.20606148C= NCBI36
NG_013086.1:g.33627C=
NG_013086.2:g.33627C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525748.6:c.1442C= MANE Select ENSP00000434364.2:p.Ala481=
ENST00000298923.11:c.*739C= ENSP00000298923.7:n.*739C=
ENST00000525748.5:c.1442C= ENSP00000434364.1:p.Ala481=
NM_004211.3:c.1442C= NP_004202.2:p.Ala481=
XM_005253225.1:c.740C= XP_005253282.1:p.Ala247=
XM_011520473.1:c.1442C= XP_011518775.1:p.Ala481=
NM_001318369.1:c.740C= NP_001305298.1:p.Ala247=
NM_004211.4:c.1442C= NP_004202.3:p.Ala481=
XM_017018544.2:c.566C= XP_016874033.1:p.Ala189=
XM_017018545.2:c.401C= XP_016874034.1:p.Ala134=
NM_001318369.2:c.740C= NP_001305298.1:p.Ala247=
NM_004211.5:c.1442C= MANE Select NP_004202.4:p.Ala481=