Canonical Allele Identifier: CA379912067
Gene: SLC6A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20601496T>G , CM000673.2:g.20601496T>G GRCh38
NC_000011.9:g.20623042T>G , CM000673.1:g.20623042T>G GRCh37
NC_000011.8:g.20579618T>G NCBI36
NG_013086.1:g.7097T>G
NG_013086.2:g.7097T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000525748.6:c.371T>G MANE Select ENSP00000434364.2:p.Phe124Cys
ENST00000298923.11:c.371T>G ENSP00000298923.7:p.Phe124Cys
ENST00000525748.5:c.371T>G ENSP00000434364.1:p.Phe124Cys
NM_004211.3:c.371T>G NP_004202.2:p.Phe124Cys
XM_005253225.1:c.-193T>G XP_005253282.1:n.-193T>G
XM_011520473.1:c.371T>G XP_011518775.1:p.Phe124Cys
NM_001318369.1:c.-193T>G NP_001305298.1:n.-193T>G
NM_004211.4:c.371T>G NP_004202.3:p.Phe124Cys
XM_017018545.2:c.-57+1821T>G XP_016874034.1:n.-57+1821T>G
NM_001318369.2:c.-193T>G NP_001305298.1:n.-193T>G
NM_004211.5:c.371T>G MANE Select NP_004202.4:p.Phe124Cys