Canonical Allele Identifier: CA350877582
Community Standard Title: NM_025243.4(SLC19A3):c.267T>G (p.Ser89Arg)
Gene: SLC19A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227699448A>C , CM000664.2:g.227699448A>C GRCh38
NC_000002.11:g.228564164A>C , CM000664.1:g.228564164A>C GRCh37
NC_000002.10:g.228272408A>C NCBI36
NG_016359.1:g.23582T>G

Transcript Alleles

HGVS Amino-acid Change
NM_025243.4:c.267T>G MANE Select NP_079519.1:p.Ser89Arg
ENST00000644224.2:c.267T>G MANE Select ENSP00000495385.1:p.Ser89Arg
NM_001371411.1:c.267T>G NP_001358340.1:p.Ser89Arg
NM_001371412.1:c.267T>G NP_001358341.1:p.Ser89Arg
NM_001371413.1:c.255T>G NP_001358342.1:p.Ser85Arg
NM_001371414.1:c.255T>G NP_001358343.1:p.Ser85Arg
NM_025243.3:c.267T>G NP_079519.1:p.Ser89Arg
ENST00000258403.7:c.267T>G ENSP00000258403.3:p.Ser89Arg
ENST00000258403.8:c.267T>G ENSP00000258403.3:p.Ser89Arg
ENST00000409287.5:c.259+8T>G ENSP00000386298.1:n.259+8T>G
ENST00000425817.5:c.267T>G ENSP00000397393.1:p.Ser89Arg
ENST00000425817.6:c.*292T>G ENSP00000397393.2:n.*292T>G
ENST00000431622.5:c.*292T>G ENSP00000400627.1:n.*292T>G
ENST00000431622.6:c.*292T>G ENSP00000400627.1:n.*292T>G
ENST00000456524.5:c.267T>G ENSP00000399001.1:p.Ser89Arg
ENST00000456524.6:c.444T>G ENSP00000399001.2:p.Ser148Arg
ENST00000642268.1:n.457T>G
ENST00000645700.1:c.151-602T>G ENSP00000495372.1:n.151-602T>G
ENST00000645923.1:c.-49T>G ENSP00000495010.1:n.-49T>G
ENST00000646591.1:c.303T>G ENSP00000496701.1:p.Ser101Arg
ENST00000647113.1:c.150+2721T>G ENSP00000494966.1:n.150+2721T>G
ENST00000676066.1:n.35-38T>G
XM_005246874.2:c.255T>G XP_005246931.1:p.Ser85Arg
XM_005246874.3:c.255T>G XP_005246931.1:p.Ser85Arg
XM_006712779.2:c.282T>G XP_006712842.1:p.Ser94Arg
XM_011511931.1:c.303T>G XP_011510233.1:p.Ser101Arg
XM_011511931.2:c.303T>G XP_011510233.1:p.Ser101Arg
XM_011511932.1:c.267T>G XP_011510234.1:p.Ser89Arg
XM_011511933.1:c.267T>G XP_011510235.1:p.Ser89Arg
XM_017005030.1:c.507T>G XP_016860519.1:p.Ser169Arg
XM_017005031.1:c.486T>G XP_016860520.1:p.Ser162Arg
XM_017005032.1:c.471T>G XP_016860521.1:p.Ser157Arg
XM_017005033.1:c.471T>G XP_016860522.1:p.Ser157Arg
XM_017005034.2:c.471T>G XP_016860523.1:p.Ser157Arg