Canonical Allele Identifier: CA364307728
Gene: SLC29A1 HGNC NCBI
POLR1C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44230850C>T , CM000668.2:g.44230850C>T GRCh38
NC_000006.11:g.44198587C>T , CM000668.1:g.44198587C>T GRCh37
NC_000006.10:g.44306565C>T NCBI36
NG_042893.1:g.16346C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371713.6:c.727C>T (SLC29A1) ENSP00000360778.1:p.Pro243Ser
ENST00000371724.6:c.727C>T (SLC29A1) ENSP00000360789.1:p.Pro243Ser
ENST00000371755.9:c.727C>T (SLC29A1) MANE Select ENSP00000360820.3:p.Pro243Ser
ENST00000393844.7:c.727C>T (SLC29A1) ENSP00000377427.1:p.Pro243Ser
ENST00000472176.2:n.1125C>T (SLC29A1)
ENST00000646251.1:c.414C>T (SLC29A1)
ENST00000651428.1:c.727C>T (SLC29A1) ENSP00000498610.1:p.Pro243Ser
ENST00000652453.1:c.727C>T (SLC29A1) ENSP00000499107.1:p.Pro243Ser
ENST00000652680.1:c.727C>T (SLC29A1) ENSP00000498747.1:p.Pro243Ser
ENST00000371708.1:c.727C>T (SLC29A1) ENSP00000360773.1:p.Pro243Ser
ENST00000371713.5:c.727C>T (SLC29A1) ENSP00000360778.1:p.Pro243Ser
ENST00000371724.5:c.727C>T (SLC29A1) ENSP00000360789.1:p.Pro243Ser
ENST00000371731.5:c.727C>T (SLC29A1) ENSP00000360796.1:p.Pro243Ser
ENST00000371740.9:c.727C>T (SLC29A1) ENSP00000360805.5:p.Pro243Ser
ENST00000371755.7:c.727C>T (SLC29A1) ENSP00000360820.3:p.Pro243Ser
ENST00000393841.5:c.727C>T (SLC29A1) ENSP00000377424.1:p.Pro243Ser
ENST00000393844.5:c.727C>T (SLC29A1) ENSP00000377427.1:p.Pro243Ser
ENST00000427851.6:c.727C>T (SLC29A1) ENSP00000392668.2:p.Pro243Ser
ENST00000472176.1:n.916C>T (SLC29A1)
NM_001078175.2:c.727C>T (SLC29A1) NP_001071643.1:p.Pro243Ser
NM_001078177.1:c.727C>T (SLC29A1) NP_001071645.1:p.Pro243Ser
NM_001304462.1:c.964C>T (SLC29A1) NP_001291391.1:p.Pro322Ser
NM_001304463.1:c.853C>T (SLC29A1) NP_001291392.1:p.Pro285Ser
NM_001304465.1:c.805C>T (SLC29A1) NP_001291394.1:p.Pro269Ser
NM_001304466.1:c.802C>T (SLC29A1) NP_001291395.1:p.Pro268Ser
XM_005248876.3:c.856C>T (SLC29A1) XP_005248933.1:p.Pro286Ser
XM_005248878.3:c.727C>T (SLC29A1) XP_005248935.1:p.Pro243Ser
XM_005248879.3:c.727C>T (SLC29A1) XP_005248936.1:p.Pro243Ser
XM_005248880.3:c.727C>T (SLC29A1) XP_005248937.1:p.Pro243Ser
XM_005248881.3:c.727C>T (SLC29A1) XP_005248938.1:p.Pro243Ser
XM_005248882.3:c.727C>T (SLC29A1) XP_005248939.1:p.Pro243Ser
XM_011514341.1:c.967C>T (SLC29A1) XP_011512643.1:p.Pro323Ser
XM_005248876.5:c.856C>T (SLC29A1) XP_005248933.1:p.Pro286Ser
XM_005248878.4:c.727C>T (SLC29A1) XP_005248935.1:p.Pro243Ser
XM_005248879.4:c.727C>T (SLC29A1) XP_005248936.1:p.Pro243Ser
XM_005248880.4:c.727C>T (SLC29A1) XP_005248937.1:p.Pro243Ser
XM_005248881.4:c.727C>T (SLC29A1) XP_005248938.1:p.Pro243Ser
XM_005248882.4:c.727C>T (SLC29A1) XP_005248939.1:p.Pro243Ser
XM_011514341.2:c.967C>T (SLC29A1) XP_011512643.1:p.Pro323Ser
XM_024446348.1:c.727C>T (SLC29A1) XP_024302116.1:p.Pro243Ser
NM_001078175.3:c.727C>T (SLC29A1) NP_001071643.1:p.Pro243Ser
NM_001078177.2:c.727C>T (SLC29A1) NP_001071645.1:p.Pro243Ser
NM_001304462.2:c.964C>T (SLC29A1) NP_001291391.1:p.Pro322Ser
NM_001304465.2:c.805C>T (SLC29A1) NP_001291394.1:p.Pro269Ser
NM_001304466.2:c.802C>T (SLC29A1) NP_001291395.1:p.Pro268Ser
NM_001372327.1:c.727C>T (SLC29A1) MANE Select NP_001359256.1:p.Pro243Ser
NM_001318876.2:c.946-211040C>T (POLR1C) NP_001305805.1:n.946-211040C>T