Canonical Allele Identifier: CA1956619736
Gene: SLC6A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20627997C= , CM000673.2:g.20627997C= GRCh38
NC_000011.9:g.20649543C= , CM000673.1:g.20649543C= GRCh37
NC_000011.8:g.20606119C= NCBI36
NG_013086.1:g.33598C=
NG_013086.2:g.33598C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525748.6:c.1413C= MANE Select ENSP00000434364.2:p.Ala471=
ENST00000298923.11:c.*710C= ENSP00000298923.7:n.*710C=
ENST00000525748.5:c.1413C= ENSP00000434364.1:p.Ala471=
NM_004211.3:c.1413C= NP_004202.2:p.Ala471=
XM_005253225.1:c.711C= XP_005253282.1:p.Ala237=
XM_011520473.1:c.1413C= XP_011518775.1:p.Ala471=
NM_001318369.1:c.711C= NP_001305298.1:p.Ala237=
NM_004211.4:c.1413C= NP_004202.3:p.Ala471=
XM_017018544.2:c.537C= XP_016874033.1:p.Ala179=
XM_017018545.2:c.372C= XP_016874034.1:p.Ala124=
NM_001318369.2:c.711C= NP_001305298.1:p.Ala237=
NM_004211.5:c.1413C= MANE Select NP_004202.4:p.Ala471=