Canonical Allele Identifier: CA1956619690
Gene: SLC6A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20627928_20627929delinsTG , CM000673.2:g.20627928_20627929delinsTG GRCh38
NC_000011.9:g.20649474_20649475delinsTG , CM000673.1:g.20649474_20649475delinsTG GRCh37
NC_000011.8:g.20606050_20606051delinsTG NCBI36
NG_013086.1:g.33529_33530delinsTG
NG_013086.2:g.33529_33530delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000525748.6:c.1396-52_1396-51delinsTG MANE Select ENSP00000434364.2:n.1396-52_1396-51delinsTG
ENST00000298923.11:c.*693-52_*693-51delinsTG ENSP00000298923.7:n.*693-52_*693-51delinsTG
ENST00000525748.5:c.1396-52_1396-51delinsTG ENSP00000434364.1:n.1396-52_1396-51delinsTG
NM_004211.3:c.1396-52_1396-51delinsTG NP_004202.2:n.1396-52_1396-51delinsTG
XM_005253225.1:c.694-52_694-51delinsTG XP_005253282.1:n.694-52_694-51delinsTG
XM_011520473.1:c.1396-52_1396-51delinsTG XP_011518775.1:n.1396-52_1396-51delinsTG
NM_001318369.1:c.694-52_694-51delinsTG NP_001305298.1:n.694-52_694-51delinsTG
NM_004211.4:c.1396-52_1396-51delinsTG NP_004202.3:n.1396-52_1396-51delinsTG
XM_017018544.2:c.520-52_520-51delinsTG XP_016874033.1:n.520-52_520-51delinsTG
XM_017018545.2:c.355-52_355-51delinsTG XP_016874034.1:n.355-52_355-51delinsTG
NM_001318369.2:c.694-52_694-51delinsTG NP_001305298.1:n.694-52_694-51delinsTG
NM_004211.5:c.1396-52_1396-51delinsTG MANE Select NP_004202.4:n.1396-52_1396-51delinsTG