Canonical Allele Identifier: CA1630848628
Gene: SLC6A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20601429G= , CM000673.2:g.20601429G= GRCh38
NC_000011.9:g.20622975G= , CM000673.1:g.20622975G= GRCh37
NC_000011.8:g.20579551G= NCBI36
NG_013086.1:g.7030G=
NG_013086.2:g.7030G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525748.6:c.304G= MANE Select ENSP00000434364.2:p.Gly102=
ENST00000298923.11:c.304G= ENSP00000298923.7:p.Gly102=
ENST00000525748.5:c.304G= ENSP00000434364.1:p.Gly102=
NM_004211.3:c.304G= NP_004202.2:p.Gly102=
XM_005253225.1:c.-260G= XP_005253282.1:n.-260G=
XM_011520473.1:c.304G= XP_011518775.1:p.Gly102=
NM_001318369.1:c.-260G= NP_001305298.1:n.-260G=
NM_004211.4:c.304G= NP_004202.3:p.Gly102=
XM_017018545.2:c.-57+1754G= XP_016874034.1:n.-57+1754G=
NM_001318369.2:c.-260G= NP_001305298.1:n.-260G=
NM_004211.5:c.304G= MANE Select NP_004202.4:p.Gly102=