Canonical Allele Identifier: CA2577266589
Gene: SLC19A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227698693G>A , CM000664.2:g.227698693G>A GRCh38
NC_000002.11:g.228563409G>A , CM000664.1:g.228563409G>A GRCh37
NC_000002.10:g.228271653G>A NCBI36
NG_016359.1:g.24337C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258403.8:c.979+43C>T ENSP00000258403.3:n.979+43C>T
ENST00000425817.6:c.*1004+43C>T ENSP00000397393.2:n.*1004+43C>T
ENST00000431622.6:c.*1004+43C>T ENSP00000400627.1:n.*1004+43C>T
ENST00000642268.1:n.1169+43C>T
ENST00000644224.2:c.979+43C>T MANE Select ENSP00000495385.1:n.979+43C>T
ENST00000645700.1:c.*90+43C>T ENSP00000495372.1:n.*90+43C>T
ENST00000645923.1:c.664+43C>T ENSP00000495010.1:n.664+43C>T
ENST00000646591.1:c.1015+43C>T ENSP00000496701.1:n.1015+43C>T
ENST00000647113.1:c.151-2612C>T ENSP00000494966.1:n.151-2612C>T
ENST00000676066.1:n.709+43C>T
ENST00000258403.7:c.979+43C>T ENSP00000258403.3:n.979+43C>T
ENST00000409287.5:c.259+763C>T ENSP00000386298.1:n.259+763C>T
ENST00000425817.5:c.979+43C>T ENSP00000397393.1:n.979+43C>T
NM_025243.3:c.979+43C>T NP_079519.1:n.979+43C>T
XM_005246874.2:c.967+43C>T XP_005246931.1:n.967+43C>T
XM_006712779.2:c.994+43C>T XP_006712842.1:n.994+43C>T
XM_011511931.1:c.1015+43C>T XP_011510233.1:n.1015+43C>T
XM_011511932.1:c.979+43C>T XP_011510234.1:n.979+43C>T
XM_011511933.1:c.979+43C>T XP_011510235.1:n.979+43C>T
XM_005246874.3:c.967+43C>T XP_005246931.1:n.967+43C>T
XM_011511931.2:c.1015+43C>T XP_011510233.1:n.1015+43C>T
XM_017005030.1:c.1219+43C>T XP_016860519.1:n.1219+43C>T
XM_017005031.1:c.1198+43C>T XP_016860520.1:n.1198+43C>T
XM_017005032.1:c.1183+43C>T XP_016860521.1:n.1183+43C>T
XM_017005033.1:c.1183+43C>T XP_016860522.1:n.1183+43C>T
XM_017005034.2:c.1183+43C>T XP_016860523.1:n.1183+43C>T
NM_025243.4:c.979+43C>T MANE Select NP_079519.1:n.979+43C>T
NM_001371411.1:c.979+43C>T NP_001358340.1:n.979+43C>T
NM_001371412.1:c.979+43C>T NP_001358341.1:n.979+43C>T
NM_001371413.1:c.967+43C>T NP_001358342.1:n.967+43C>T
NM_001371414.1:c.967+43C>T NP_001358343.1:n.967+43C>T