Canonical Allele Identifier: CA935753244
Gene: SLC6A5 HGNC NCBI

Linked Data

dbSNP Id: rs1853028208

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20627834del , CM000673.2:g.20627834del GRCh38
NC_000011.9:g.20649380del , CM000673.1:g.20649380del GRCh37
NC_000011.8:g.20605956del NCBI36
NG_013086.1:g.33435del
NG_013086.2:g.33435del

Transcript Alleles

HGVS Amino-acid Change
ENST00000525748.6:c.1396-146del MANE Select ENSP00000434364.2:n.1396-146del
ENST00000298923.11:c.*693-146del ENSP00000298923.7:n.*693-146del
ENST00000525748.5:c.1396-146del ENSP00000434364.1:n.1396-146del
NM_004211.3:c.1396-146del NP_004202.2:n.1396-146del
XM_005253225.1:c.694-146del XP_005253282.1:n.694-146del
XM_011520473.1:c.1396-146del XP_011518775.1:n.1396-146del
NM_001318369.1:c.694-146del NP_001305298.1:n.694-146del
NM_004211.4:c.1396-146del NP_004202.3:n.1396-146del
XM_017018544.2:c.520-146del XP_016874033.1:n.520-146del
XM_017018545.2:c.355-146del XP_016874034.1:n.355-146del
NM_001318369.2:c.694-146del NP_001305298.1:n.694-146del
NM_004211.5:c.1396-146del MANE Select NP_004202.4:n.1396-146del