Canonical Allele Identifier: CA2149257

Gene: SLC19A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227699102T>C , CM000664.2:g.227699102T>C	GRCh38
NC_000002.11:g.228563818T>C , CM000664.1:g.228563818T>C	GRCh37
NC_000002.10:g.228272062T>C	NCBI36
NG_016359.1:g.23928A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025243.4:c.613A>G MANE Select	NP_079519.1:p.Arg205Gly
ENST00000644224.2:c.613A>G MANE Select	ENSP00000495385.1:p.Arg205Gly
NM_001371411.1:c.613A>G	NP_001358340.1:p.Arg205Gly
NM_001371412.1:c.613A>G	NP_001358341.1:p.Arg205Gly
NM_001371413.1:c.601A>G	NP_001358342.1:p.Arg201Gly
NM_001371414.1:c.601A>G	NP_001358343.1:p.Arg201Gly
NM_025243.3:c.613A>G	NP_079519.1:p.Arg205Gly
ENST00000258403.7:c.613A>G	ENSP00000258403.3:p.Arg205Gly
ENST00000258403.8:c.613A>G	ENSP00000258403.3:p.Arg205Gly
ENST00000409287.5:c.259+354A>G	ENSP00000386298.1:n.259+354A>G
ENST00000425817.5:c.613A>G	ENSP00000397393.1:p.Arg205Gly
ENST00000425817.6:c.*638A>G	ENSP00000397393.2:n.*638A>G
ENST00000431622.6:c.*638A>G	ENSP00000400627.1:n.*638A>G
ENST00000642268.1:n.803A>G
ENST00000645700.1:c.151-256A>G	ENSP00000495372.1:n.151-256A>G
ENST00000645923.1:c.298A>G	ENSP00000495010.1:p.Arg100Gly
ENST00000646591.1:c.649A>G	ENSP00000496701.1:p.Arg217Gly
ENST00000647113.1:c.151-3021A>G	ENSP00000494966.1:n.151-3021A>G
ENST00000676066.1:n.343A>G
XM_005246874.2:c.601A>G	XP_005246931.1:p.Arg201Gly
XM_005246874.3:c.601A>G	XP_005246931.1:p.Arg201Gly
XM_006712779.2:c.628A>G	XP_006712842.1:p.Arg210Gly
XM_011511931.1:c.649A>G	XP_011510233.1:p.Arg217Gly
XM_011511931.2:c.649A>G	XP_011510233.1:p.Arg217Gly
XM_011511932.1:c.613A>G	XP_011510234.1:p.Arg205Gly
XM_011511933.1:c.613A>G	XP_011510235.1:p.Arg205Gly
XM_017005030.1:c.853A>G	XP_016860519.1:p.Arg285Gly
XM_017005031.1:c.832A>G	XP_016860520.1:p.Arg278Gly
XM_017005032.1:c.817A>G	XP_016860521.1:p.Arg273Gly
XM_017005033.1:c.817A>G	XP_016860522.1:p.Arg273Gly
XM_017005034.2:c.817A>G	XP_016860523.1:p.Arg273Gly