Canonical Allele Identifier: CA350877741
Community Standard Title: NM_025243.4(SLC19A3):c.189C>G (p.Tyr63Ter)
Gene: SLC19A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227699526G>C , CM000664.2:g.227699526G>C GRCh38
NC_000002.11:g.228564242G>C , CM000664.1:g.228564242G>C GRCh37
NC_000002.10:g.228272486G>C NCBI36
NG_016359.1:g.23504C>G

Transcript Alleles

HGVS Amino-acid Change
NM_025243.4:c.189C>G MANE Select NP_079519.1:p.Tyr63Ter
ENST00000644224.2:c.189C>G MANE Select ENSP00000495385.1:p.Tyr63Ter
NM_001371411.1:c.189C>G NP_001358340.1:p.Tyr63Ter
NM_001371412.1:c.189C>G NP_001358341.1:p.Tyr63Ter
NM_001371413.1:c.177C>G NP_001358342.1:p.Tyr59Ter
NM_001371414.1:c.177C>G NP_001358343.1:p.Tyr59Ter
NM_025243.3:c.189C>G NP_079519.1:p.Tyr63Ter
ENST00000258403.7:c.189C>G ENSP00000258403.3:p.Tyr63Ter
ENST00000258403.8:c.189C>G ENSP00000258403.3:p.Tyr63Ter
ENST00000409287.5:c.189C>G ENSP00000386298.1:p.Tyr63Ter
ENST00000419059.1:c.189C>G ENSP00000398349.1:p.Tyr63Ter
ENST00000425817.5:c.189C>G ENSP00000397393.1:p.Tyr63Ter
ENST00000425817.6:c.*214C>G ENSP00000397393.2:n.*214C>G
ENST00000431622.5:c.*214C>G ENSP00000400627.1:n.*214C>G
ENST00000431622.6:c.*214C>G ENSP00000400627.1:n.*214C>G
ENST00000456524.5:c.189C>G ENSP00000399001.1:p.Tyr63Ter
ENST00000456524.6:c.366C>G ENSP00000399001.2:p.Tyr122Ter
ENST00000642268.1:n.379C>G
ENST00000645700.1:c.151-680C>G ENSP00000495372.1:n.151-680C>G
ENST00000645923.1:c.-127C>G ENSP00000495010.1:n.-127C>G
ENST00000646591.1:c.225C>G ENSP00000496701.1:p.Tyr75Ter
ENST00000647113.1:c.150+2643C>G ENSP00000494966.1:n.150+2643C>G
ENST00000676066.1:n.35-116C>G
XM_005246874.2:c.177C>G XP_005246931.1:p.Tyr59Ter
XM_005246874.3:c.177C>G XP_005246931.1:p.Tyr59Ter
XM_006712779.2:c.204C>G XP_006712842.1:p.Tyr68Ter
XM_011511931.1:c.225C>G XP_011510233.1:p.Tyr75Ter
XM_011511931.2:c.225C>G XP_011510233.1:p.Tyr75Ter
XM_011511932.1:c.189C>G XP_011510234.1:p.Tyr63Ter
XM_011511933.1:c.189C>G XP_011510235.1:p.Tyr63Ter
XM_017005030.1:c.429C>G XP_016860519.1:p.Tyr143Ter
XM_017005031.1:c.408C>G XP_016860520.1:p.Tyr136Ter
XM_017005032.1:c.393C>G XP_016860521.1:p.Tyr131Ter
XM_017005033.1:c.393C>G XP_016860522.1:p.Tyr131Ter
XM_017005034.2:c.393C>G XP_016860523.1:p.Tyr131Ter