Canonical Allele Identifier: CA379913908
Community Standard Title: NM_004211.5(SLC6A5):c.811+1G>T
Gene: SLC6A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20607139G>T , CM000673.2:g.20607139G>T GRCh38
NC_000011.9:g.20628685G>T , CM000673.1:g.20628685G>T GRCh37
NC_000011.8:g.20585261G>T NCBI36
NG_013086.1:g.12740G>T
NG_013086.2:g.12740G>T

Transcript Alleles

HGVS Amino-acid Change
NM_004211.5:c.811+1G>T MANE Select NP_004202.4:n.811+1G>T
ENST00000525748.6:c.811+1G>T MANE Select ENSP00000434364.2:n.811+1G>T
NM_001318369.1:c.109+1G>T NP_001305298.1:n.109+1G>T
NM_001318369.2:c.109+1G>T NP_001305298.1:n.109+1G>T
NM_004211.3:c.811+1G>T NP_004202.2:n.811+1G>T
NM_004211.4:c.811+1G>T NP_004202.3:n.811+1G>T
ENST00000298923.11:c.*108+1G>T ENSP00000298923.7:n.*108+1G>T
ENST00000525748.5:c.811+1G>T ENSP00000434364.1:n.811+1G>T
XM_005253225.1:c.109+1G>T XP_005253282.1:n.109+1G>T
XM_011520473.1:c.811+1G>T XP_011518775.1:n.811+1G>T
XM_017018544.2:c.109+1G>T XP_016874033.1:n.109+1G>T
XM_017018545.2:c.-57+7464G>T XP_016874034.1:n.-57+7464G>T