Canonical Allele Identifier: CA364306059
Gene: SLC29A1 HGNC NCBI
POLR1C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44230366G>T , CM000668.2:g.44230366G>T GRCh38
NC_000006.11:g.44198103G>T , CM000668.1:g.44198103G>T GRCh37
NC_000006.10:g.44306081G>T NCBI36
NG_042893.1:g.15862G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371713.6:c.474G>T (SLC29A1) ENSP00000360778.1:p.Gln158His
ENST00000371724.6:c.474G>T (SLC29A1) ENSP00000360789.1:p.Gln158His
ENST00000371731.6:c.474G>T (SLC29A1) ENSP00000360796.2:p.Gln158His
ENST00000371740.10:c.474G>T (SLC29A1) ENSP00000360805.6:p.Gln158His
ENST00000371755.9:c.474G>T (SLC29A1) MANE Select ENSP00000360820.3:p.Gln158His
ENST00000393841.6:c.474G>T (SLC29A1) ENSP00000377424.2:p.Gln158His
ENST00000393844.7:c.474G>T (SLC29A1) ENSP00000377427.1:p.Gln158His
ENST00000472176.2:n.872G>T (SLC29A1)
ENST00000642613.1:n.892G>T (SLC29A1)
ENST00000643028.2:c.417G>T (SLC29A1) ENSP00000495211.2:p.Gln139His
ENST00000646251.1:c.162-1G>T (SLC29A1)
ENST00000646582.1:c.474G>T (SLC29A1) ENSP00000496745.1:p.Gln158His
ENST00000647460.1:c.474G>T (SLC29A1) ENSP00000496479.1:p.Gln158His
ENST00000651428.1:c.474G>T (SLC29A1) ENSP00000498610.1:p.Gln158His
ENST00000652453.1:c.474G>T (SLC29A1) ENSP00000499107.1:p.Gln158His
ENST00000652680.1:c.474G>T (SLC29A1) ENSP00000498747.1:p.Gln158His
ENST00000371708.1:c.474G>T (SLC29A1) ENSP00000360773.1:p.Gln158His
ENST00000371713.5:c.474G>T (SLC29A1) ENSP00000360778.1:p.Gln158His
ENST00000371724.5:c.474G>T (SLC29A1) ENSP00000360789.1:p.Gln158His
ENST00000371731.5:c.474G>T (SLC29A1) ENSP00000360796.1:p.Gln158His
ENST00000371740.9:c.474G>T (SLC29A1) ENSP00000360805.5:p.Gln158His
ENST00000371755.7:c.474G>T (SLC29A1) ENSP00000360820.3:p.Gln158His
ENST00000393841.5:c.474G>T (SLC29A1) ENSP00000377424.1:p.Gln158His
ENST00000393844.5:c.474G>T (SLC29A1) ENSP00000377427.1:p.Gln158His
ENST00000427851.6:c.474G>T (SLC29A1) ENSP00000392668.2:p.Gln158His
ENST00000472176.1:n.663G>T (SLC29A1)
NM_001078175.2:c.474G>T (SLC29A1) NP_001071643.1:p.Gln158His
NM_001078177.1:c.474G>T (SLC29A1) NP_001071645.1:p.Gln158His
NM_001304462.1:c.711G>T (SLC29A1) NP_001291391.1:p.Gln237His
NM_001304463.1:c.600G>T (SLC29A1) NP_001291392.1:p.Gln200His
NM_001304465.1:c.552G>T (SLC29A1) NP_001291394.1:p.Gln184His
NM_001304466.1:c.549G>T (SLC29A1) NP_001291395.1:p.Gln183His
XM_005248876.3:c.603G>T (SLC29A1) XP_005248933.1:p.Gln201His
XM_005248878.3:c.474G>T (SLC29A1) XP_005248935.1:p.Gln158His
XM_005248879.3:c.474G>T (SLC29A1) XP_005248936.1:p.Gln158His
XM_005248880.3:c.474G>T (SLC29A1) XP_005248937.1:p.Gln158His
XM_005248881.3:c.474G>T (SLC29A1) XP_005248938.1:p.Gln158His
XM_005248882.3:c.474G>T (SLC29A1) XP_005248939.1:p.Gln158His
XM_011514341.1:c.714G>T (SLC29A1) XP_011512643.1:p.Gln238His
XM_005248876.5:c.603G>T (SLC29A1) XP_005248933.1:p.Gln201His
XM_005248878.4:c.474G>T (SLC29A1) XP_005248935.1:p.Gln158His
XM_005248879.4:c.474G>T (SLC29A1) XP_005248936.1:p.Gln158His
XM_005248880.4:c.474G>T (SLC29A1) XP_005248937.1:p.Gln158His
XM_005248881.4:c.474G>T (SLC29A1) XP_005248938.1:p.Gln158His
XM_005248882.4:c.474G>T (SLC29A1) XP_005248939.1:p.Gln158His
XM_011514341.2:c.714G>T (SLC29A1) XP_011512643.1:p.Gln238His
XM_024446348.1:c.474G>T (SLC29A1) XP_024302116.1:p.Gln158His
NM_001078175.3:c.474G>T (SLC29A1) NP_001071643.1:p.Gln158His
NM_001078177.2:c.474G>T (SLC29A1) NP_001071645.1:p.Gln158His
NM_001304462.2:c.711G>T (SLC29A1) NP_001291391.1:p.Gln237His
NM_001304465.2:c.552G>T (SLC29A1) NP_001291394.1:p.Gln184His
NM_001304466.2:c.549G>T (SLC29A1) NP_001291395.1:p.Gln183His
NM_001372327.1:c.474G>T (SLC29A1) MANE Select NP_001359256.1:p.Gln158His
NM_001318876.2:c.946-211524G>T (POLR1C) NP_001305805.1:n.946-211524G>T