Canonical Allele Identifier: CA5921035
Gene: SLC6A5 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000525748.6:c.304G>A MANE Select ENSP00000434364.2:p.Gly102Ser
ENST00000298923.11:c.304G>A ENSP00000298923.7:p.Gly102Ser
ENST00000525748.5:c.304G>A ENSP00000434364.1:p.Gly102Ser
NM_004211.3:c.304G>A NP_004202.2:p.Gly102Ser
XM_005253225.1:c.-260G>A XP_005253282.1:n.-260G>A
XM_011520473.1:c.304G>A XP_011518775.1:p.Gly102Ser
NM_001318369.1:c.-260G>A NP_001305298.1:n.-260G>A
NM_004211.4:c.304G>A NP_004202.3:p.Gly102Ser
XM_017018545.2:c.-57+1754G>A XP_016874034.1:n.-57+1754G>A
NM_001318369.2:c.-260G>A NP_001305298.1:n.-260G>A
NM_004211.5:c.304G>A MANE Select NP_004202.4:p.Gly102Ser