Canonical Allele Identifier: CA2149094

Gene: SLC19A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227687545A>G , CM000664.2:g.227687545A>G	GRCh38
NC_000002.11:g.228552261A>G , CM000664.1:g.228552261A>G	GRCh37
NC_000002.10:g.228260505A>G	NCBI36
NG_016359.1:g.35485T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_025243.4:c.1343T>C MANE Select	NP_079519.1:p.Val448Ala
ENST00000644224.2:c.1343T>C MANE Select	ENSP00000495385.1:p.Val448Ala
NM_001371411.1:c.1343T>C	NP_001358340.1:p.Val448Ala
NM_001371412.1:c.1343T>C	NP_001358341.1:p.Val448Ala
NM_001371413.1:c.1331T>C	NP_001358342.1:p.Val444Ala
NM_001371414.1:c.1331T>C	NP_001358343.1:p.Val444Ala
NM_025243.3:c.1343T>C	NP_079519.1:p.Val448Ala
ENST00000258403.7:c.1343T>C	ENSP00000258403.3:p.Val448Ala
ENST00000258403.8:c.1343T>C	ENSP00000258403.3:p.Val448Ala
ENST00000409287.5:c.260-1376T>C	ENSP00000386298.1:n.260-1376T>C
ENST00000425817.5:c.1343T>C	ENSP00000397393.1:p.Val448Ala
ENST00000425817.6:c.*1368T>C	ENSP00000397393.2:n.*1368T>C
ENST00000431622.6:c.*1368T>C	ENSP00000400627.1:n.*1368T>C
ENST00000642268.1:n.1533T>C
ENST00000645700.1:c.*454T>C	ENSP00000495372.1:n.*454T>C
ENST00000645923.1:c.*537T>C	ENSP00000495010.1:n.*537T>C
ENST00000646591.1:c.1379T>C	ENSP00000496701.1:p.Val460Ala
ENST00000647113.1:c.*331T>C	ENSP00000494966.1:n.*331T>C
ENST00000676066.1:n.1073T>C
XM_005246874.2:c.1331T>C	XP_005246931.1:p.Val444Ala
XM_005246874.3:c.1331T>C	XP_005246931.1:p.Val444Ala
XM_006712779.2:c.1358T>C	XP_006712842.1:p.Val453Ala
XM_011511931.1:c.1379T>C	XP_011510233.1:p.Val460Ala
XM_011511931.2:c.1379T>C	XP_011510233.1:p.Val460Ala
XM_011511932.1:c.1343T>C	XP_011510234.1:p.Val448Ala
XM_011511933.1:c.1343T>C	XP_011510235.1:p.Val448Ala
XM_017005030.1:c.1583T>C	XP_016860519.1:p.Val528Ala
XM_017005031.1:c.1562T>C	XP_016860520.1:p.Val521Ala
XM_017005032.1:c.1547T>C	XP_016860521.1:p.Val516Ala
XM_017005033.1:c.1547T>C	XP_016860522.1:p.Val516Ala
XM_017005034.2:c.1547T>C	XP_016860523.1:p.Val516Ala