Canonical Allele Identifier: CA2149163

Gene: SLC19A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227696005G>C , CM000664.2:g.227696005G>C	GRCh38
NC_000002.11:g.228560721G>C , CM000664.1:g.228560721G>C	GRCh37
NC_000002.10:g.228268965G>C	NCBI36
NG_016359.1:g.27025C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025243.4:c.1056C>G MANE Select	NP_079519.1:p.Phe352Leu
ENST00000644224.2:c.1056C>G MANE Select	ENSP00000495385.1:p.Phe352Leu
NM_001371411.1:c.1056C>G	NP_001358340.1:p.Phe352Leu
NM_001371412.1:c.1056C>G	NP_001358341.1:p.Phe352Leu
NM_001371413.1:c.1044C>G	NP_001358342.1:p.Phe348Leu
NM_001371414.1:c.1044C>G	NP_001358343.1:p.Phe348Leu
NM_025243.3:c.1056C>G	NP_079519.1:p.Phe352Leu
ENST00000258403.7:c.1056C>G	ENSP00000258403.3:p.Phe352Leu
ENST00000258403.8:c.1056C>G	ENSP00000258403.3:p.Phe352Leu
ENST00000409287.5:c.259+3451C>G	ENSP00000386298.1:n.259+3451C>G
ENST00000425817.5:c.1056C>G	ENSP00000397393.1:p.Phe352Leu
ENST00000425817.6:c.*1081C>G	ENSP00000397393.2:n.*1081C>G
ENST00000431622.6:c.*1081C>G	ENSP00000400627.1:n.*1081C>G
ENST00000642268.1:n.1246C>G
ENST00000645700.1:c.*167C>G	ENSP00000495372.1:n.*167C>G
ENST00000645923.1:c.741C>G	ENSP00000495010.1:p.Phe247Leu
ENST00000646591.1:c.1092C>G	ENSP00000496701.1:p.Phe364Leu
ENST00000647113.1:c.*44C>G	ENSP00000494966.1:n.*44C>G
ENST00000676066.1:n.786C>G
XM_005246874.2:c.1044C>G	XP_005246931.1:p.Phe348Leu
XM_005246874.3:c.1044C>G	XP_005246931.1:p.Phe348Leu
XM_006712779.2:c.1071C>G	XP_006712842.1:p.Phe357Leu
XM_011511931.1:c.1092C>G	XP_011510233.1:p.Phe364Leu
XM_011511931.2:c.1092C>G	XP_011510233.1:p.Phe364Leu
XM_011511932.1:c.1056C>G	XP_011510234.1:p.Phe352Leu
XM_011511933.1:c.1056C>G	XP_011510235.1:p.Phe352Leu
XM_017005030.1:c.1296C>G	XP_016860519.1:p.Phe432Leu
XM_017005031.1:c.1275C>G	XP_016860520.1:p.Phe425Leu
XM_017005032.1:c.1260C>G	XP_016860521.1:p.Phe420Leu
XM_017005033.1:c.1260C>G	XP_016860522.1:p.Phe420Leu
XM_017005034.2:c.1260C>G	XP_016860523.1:p.Phe420Leu