Canonical Allele Identifier: CA2149397

Gene: SLC19A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227702167A>G , CM000664.2:g.227702167A>G	GRCh38
NC_000002.11:g.228566883A>G , CM000664.1:g.228566883A>G	GRCh37
NC_000002.10:g.228275127A>G	NCBI36
NG_016359.1:g.20863T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_025243.4:c.150+2T>C MANE Select	NP_079519.1:n.150+2T>C
ENST00000644224.2:c.150+2T>C MANE Select	ENSP00000495385.1:n.150+2T>C
NM_001371411.1:c.150+2T>C	NP_001358340.1:n.150+2T>C
NM_001371412.1:c.150+2T>C	NP_001358341.1:n.150+2T>C
NM_001371413.1:c.-59+2T>C	NP_001358342.1:n.-59+2T>C
NM_001371414.1:c.-59+2T>C	NP_001358343.1:n.-59+2T>C
NM_025243.3:c.150+2T>C	NP_079519.1:n.150+2T>C
ENST00000258403.7:c.150+2T>C	ENSP00000258403.3:n.150+2T>C
ENST00000258403.8:c.150+2T>C	ENSP00000258403.3:n.150+2T>C
ENST00000409287.5:c.150+2T>C	ENSP00000386298.1:n.150+2T>C
ENST00000409456.2:c.150+2T>C	ENSP00000387193.2:n.150+2T>C
ENST00000419059.1:c.150+2T>C	ENSP00000398349.1:n.150+2T>C
ENST00000425817.5:c.150+2T>C	ENSP00000397393.1:n.150+2T>C
ENST00000425817.6:c.150+2T>C	ENSP00000397393.2:n.150+2T>C
ENST00000431622.5:c.150+2T>C	ENSP00000400627.1:n.150+2T>C
ENST00000431622.6:c.150+2T>C	ENSP00000400627.1:n.150+2T>C
ENST00000456524.5:c.150+2T>C	ENSP00000399001.1:n.150+2T>C
ENST00000456524.6:c.327+2T>C	ENSP00000399001.2:n.327+2T>C
ENST00000477697.1:n.211T>C
ENST00000645700.1:c.150+2T>C	ENSP00000495372.1:n.150+2T>C
ENST00000645923.1:c.-165-2603T>C	ENSP00000495010.1:n.-165-2603T>C
ENST00000646591.1:c.186+2T>C	ENSP00000496701.1:n.186+2T>C
ENST00000647113.1:c.150+2T>C	ENSP00000494966.1:n.150+2T>C
XM_005246874.2:c.-59+2T>C	XP_005246931.1:n.-59+2T>C
XM_005246874.3:c.-59+2T>C	XP_005246931.1:n.-59+2T>C
XM_006712779.2:c.165+2T>C	XP_006712842.1:n.165+2T>C
XM_011511931.1:c.186+2T>C	XP_011510233.1:n.186+2T>C
XM_011511931.2:c.186+2T>C	XP_011510233.1:n.186+2T>C
XM_011511932.1:c.150+2T>C	XP_011510234.1:n.150+2T>C
XM_011511933.1:c.150+2T>C	XP_011510235.1:n.150+2T>C
XM_017005030.1:c.186+2T>C	XP_016860519.1:n.186+2T>C
XM_017005031.1:c.165+2T>C	XP_016860520.1:n.165+2T>C
XM_017005032.1:c.150+2T>C	XP_016860521.1:n.150+2T>C
XM_017005033.1:c.150+2T>C	XP_016860522.1:n.150+2T>C
XM_017005034.2:c.150+2T>C	XP_016860523.1:n.150+2T>C