Canonical Allele Identifier: CA1956619710
Gene: SLC6A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20627966_20627967delinsCT , CM000673.2:g.20627966_20627967delinsCT GRCh38
NC_000011.9:g.20649512_20649513delinsCT , CM000673.1:g.20649512_20649513delinsCT GRCh37
NC_000011.8:g.20606088_20606089delinsCT NCBI36
NG_013086.1:g.33567_33568delinsCT
NG_013086.2:g.33567_33568delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000525748.6:c.1396-14_1396-13delinsCT MANE Select ENSP00000434364.2:n.1396-14_1396-13delinsCT
ENST00000298923.11:c.*693-14_*693-13delinsCT ENSP00000298923.7:n.*693-14_*693-13delinsCT
ENST00000525748.5:c.1396-14_1396-13delinsCT ENSP00000434364.1:n.1396-14_1396-13delinsCT
NM_004211.3:c.1396-14_1396-13delinsCT NP_004202.2:n.1396-14_1396-13delinsCT
XM_005253225.1:c.694-14_694-13delinsCT XP_005253282.1:n.694-14_694-13delinsCT
XM_011520473.1:c.1396-14_1396-13delinsCT XP_011518775.1:n.1396-14_1396-13delinsCT
NM_001318369.1:c.694-14_694-13delinsCT NP_001305298.1:n.694-14_694-13delinsCT
NM_004211.4:c.1396-14_1396-13delinsCT NP_004202.3:n.1396-14_1396-13delinsCT
XM_017018544.2:c.520-14_520-13delinsCT XP_016874033.1:n.520-14_520-13delinsCT
XM_017018545.2:c.355-14_355-13delinsCT XP_016874034.1:n.355-14_355-13delinsCT
NM_001318369.2:c.694-14_694-13delinsCT NP_001305298.1:n.694-14_694-13delinsCT
NM_004211.5:c.1396-14_1396-13delinsCT MANE Select NP_004202.4:n.1396-14_1396-13delinsCT