Canonical Allele Identifier: CA322152

Gene: SLC19A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227699158A>G , CM000664.2:g.227699158A>G	GRCh38
NC_000002.11:g.228563874A>G , CM000664.1:g.228563874A>G	GRCh37
NC_000002.10:g.228272118A>G	NCBI36
NG_016359.1:g.23872T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_025243.4:c.557T>C MANE Select	NP_079519.1:p.Phe186Ser
ENST00000644224.2:c.557T>C MANE Select	ENSP00000495385.1:p.Phe186Ser
NM_001371411.1:c.557T>C	NP_001358340.1:p.Phe186Ser
NM_001371412.1:c.557T>C	NP_001358341.1:p.Phe186Ser
NM_001371413.1:c.545T>C	NP_001358342.1:p.Phe182Ser
NM_001371414.1:c.545T>C	NP_001358343.1:p.Phe182Ser
NM_025243.3:c.557T>C	NP_079519.1:p.Phe186Ser
ENST00000258403.7:c.557T>C	ENSP00000258403.3:p.Phe186Ser
ENST00000258403.8:c.557T>C	ENSP00000258403.3:p.Phe186Ser
ENST00000409287.5:c.259+298T>C	ENSP00000386298.1:n.259+298T>C
ENST00000425817.5:c.557T>C	ENSP00000397393.1:p.Phe186Ser
ENST00000425817.6:c.*582T>C	ENSP00000397393.2:n.*582T>C
ENST00000431622.6:c.*582T>C	ENSP00000400627.1:n.*582T>C
ENST00000642268.1:n.747T>C
ENST00000645700.1:c.151-312T>C	ENSP00000495372.1:n.151-312T>C
ENST00000645923.1:c.242T>C	ENSP00000495010.1:p.Phe81Ser
ENST00000646591.1:c.593T>C	ENSP00000496701.1:p.Phe198Ser
ENST00000647113.1:c.150+3011T>C	ENSP00000494966.1:n.150+3011T>C
ENST00000676066.1:n.287T>C
XM_005246874.2:c.545T>C	XP_005246931.1:p.Phe182Ser
XM_005246874.3:c.545T>C	XP_005246931.1:p.Phe182Ser
XM_006712779.2:c.572T>C	XP_006712842.1:p.Phe191Ser
XM_011511931.1:c.593T>C	XP_011510233.1:p.Phe198Ser
XM_011511931.2:c.593T>C	XP_011510233.1:p.Phe198Ser
XM_011511932.1:c.557T>C	XP_011510234.1:p.Phe186Ser
XM_011511933.1:c.557T>C	XP_011510235.1:p.Phe186Ser
XM_017005030.1:c.797T>C	XP_016860519.1:p.Phe266Ser
XM_017005031.1:c.776T>C	XP_016860520.1:p.Phe259Ser
XM_017005032.1:c.761T>C	XP_016860521.1:p.Phe254Ser
XM_017005033.1:c.761T>C	XP_016860522.1:p.Phe254Ser
XM_017005034.2:c.761T>C	XP_016860523.1:p.Phe254Ser