Canonical Allele Identifier: CA1956619748
Gene: SLC6A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20628027A= , CM000673.2:g.20628027A= GRCh38
NC_000011.9:g.20649573A= , CM000673.1:g.20649573A= GRCh37
NC_000011.8:g.20606149A= NCBI36
NG_013086.1:g.33628A=
NG_013086.2:g.33628A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525748.6:c.1443A= MANE Select ENSP00000434364.2:p.Ala481=
ENST00000298923.11:c.*740A= ENSP00000298923.7:n.*740A=
ENST00000525748.5:c.1443A= ENSP00000434364.1:p.Ala481=
NM_004211.3:c.1443A= NP_004202.2:p.Ala481=
XM_005253225.1:c.741A= XP_005253282.1:p.Ala247=
XM_011520473.1:c.1443A= XP_011518775.1:p.Ala481=
NM_001318369.1:c.741A= NP_001305298.1:p.Ala247=
NM_004211.4:c.1443A= NP_004202.3:p.Ala481=
XM_017018544.2:c.567A= XP_016874033.1:p.Ala189=
XM_017018545.2:c.402A= XP_016874034.1:p.Ala134=
NM_001318369.2:c.741A= NP_001305298.1:p.Ala247=
NM_004211.5:c.1443A= MANE Select NP_004202.4:p.Ala481=