Canonical Allele Identifier: CA2149306

Gene: SLC19A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227699316G>C , CM000664.2:g.227699316G>C	GRCh38
NC_000002.11:g.228564032G>C , CM000664.1:g.228564032G>C	GRCh37
NC_000002.10:g.228272276G>C	NCBI36
NG_016359.1:g.23714C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025243.4:c.399C>G MANE Select	NP_079519.1:p.Pro133=
ENST00000644224.2:c.399C>G MANE Select	ENSP00000495385.1:p.Pro133=
NM_001371411.1:c.399C>G	NP_001358340.1:p.Pro133=
NM_001371412.1:c.399C>G	NP_001358341.1:p.Pro133=
NM_001371413.1:c.387C>G	NP_001358342.1:p.Pro129=
NM_001371414.1:c.387C>G	NP_001358343.1:p.Pro129=
NM_025243.3:c.399C>G	NP_079519.1:p.Pro133=
ENST00000258403.7:c.399C>G	ENSP00000258403.3:p.Pro133=
ENST00000258403.8:c.399C>G	ENSP00000258403.3:p.Pro133=
ENST00000409287.5:c.259+140C>G	ENSP00000386298.1:n.259+140C>G
ENST00000425817.5:c.399C>G	ENSP00000397393.1:p.Pro133=
ENST00000425817.6:c.*424C>G	ENSP00000397393.2:n.*424C>G
ENST00000431622.6:c.*424C>G	ENSP00000400627.1:n.*424C>G
ENST00000456524.6:c.576C>G	ENSP00000399001.2:p.Pro192=
ENST00000642268.1:n.589C>G
ENST00000645700.1:c.151-470C>G	ENSP00000495372.1:n.151-470C>G
ENST00000645923.1:c.84C>G	ENSP00000495010.1:p.Pro28=
ENST00000646591.1:c.435C>G	ENSP00000496701.1:p.Pro145=
ENST00000647113.1:c.150+2853C>G	ENSP00000494966.1:n.150+2853C>G
ENST00000676066.1:n.129C>G
XM_005246874.2:c.387C>G	XP_005246931.1:p.Pro129=
XM_005246874.3:c.387C>G	XP_005246931.1:p.Pro129=
XM_006712779.2:c.414C>G	XP_006712842.1:p.Pro138=
XM_011511931.1:c.435C>G	XP_011510233.1:p.Pro145=
XM_011511931.2:c.435C>G	XP_011510233.1:p.Pro145=
XM_011511932.1:c.399C>G	XP_011510234.1:p.Pro133=
XM_011511933.1:c.399C>G	XP_011510235.1:p.Pro133=
XM_017005030.1:c.639C>G	XP_016860519.1:p.Pro213=
XM_017005031.1:c.618C>G	XP_016860520.1:p.Pro206=
XM_017005032.1:c.603C>G	XP_016860521.1:p.Pro201=
XM_017005033.1:c.603C>G	XP_016860522.1:p.Pro201=
XM_017005034.2:c.603C>G	XP_016860523.1:p.Pro201=