Canonical Allele Identifier: CA2612829935
Gene: SLC6A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20638431G>A , CM000673.2:g.20638431G>A GRCh38
NC_000011.9:g.20659977G>A , CM000673.1:g.20659977G>A GRCh37
NC_000011.8:g.20616553G>A NCBI36
NG_013086.1:g.44032G>A
NG_013086.2:g.44032G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000525748.6:c.1870-28G>A MANE Select ENSP00000434364.2:n.1870-28G>A
ENST00000298923.11:c.*1167-28G>A ENSP00000298923.7:n.*1167-28G>A
ENST00000525748.5:c.1870-28G>A ENSP00000434364.1:n.1870-28G>A
ENST00000528440.1:n.401-28G>A
NM_004211.3:c.1870-28G>A NP_004202.2:n.1870-28G>A
XM_005253225.1:c.1168-28G>A XP_005253282.1:n.1168-28G>A
XM_011520473.1:c.1870-28G>A XP_011518775.1:n.1870-28G>A
NM_001318369.1:c.1168-28G>A NP_001305298.1:n.1168-28G>A
NM_004211.4:c.1870-28G>A NP_004202.3:n.1870-28G>A
XM_017018544.2:c.994-28G>A XP_016874033.1:n.994-28G>A
XM_017018545.2:c.829-28G>A XP_016874034.1:n.829-28G>A
NM_001318369.2:c.1168-28G>A NP_001305298.1:n.1168-28G>A
NM_004211.5:c.1870-28G>A MANE Select NP_004202.4:n.1870-28G>A