Canonical Allele Identifier: CA367192797
Gene: NT5C3A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.33021334A>T , CM000669.2:g.33021334A>T GRCh38
NC_000007.13:g.33060946A>T , CM000669.1:g.33060946A>T GRCh37
NC_000007.12:g.33027471A>T NCBI36
NG_015800.1:g.46464T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409467.6:c.240T>A ENSP00000387166.1:p.Tyr80Ter
ENST00000610140.7:c.378T>A MANE Select ENSP00000476480.2:p.Tyr126Ter
ENST00000643244.1:c.276T>A ENSP00000496364.1:p.Tyr92Ter
ENST00000242210.11:c.393T>A ENSP00000242210.7:p.Tyr131Ter
ENST00000381626.6:c.240T>A ENSP00000371039.2:p.Tyr80Ter
ENST00000396152.6:c.276T>A ENSP00000379456.2:p.Tyr92Ter
ENST00000405342.5:c.276T>A ENSP00000385261.1:p.Tyr92Ter
ENST00000409467.5:c.240T>A ENSP00000387166.1:p.Tyr80Ter
ENST00000409787.4:c.276T>A ENSP00000387205.1:p.Tyr92Ter
ENST00000456458.5:c.*283T>A ENSP00000389676.2:n.*283T>A
ENST00000610140.5:c.378T>A ENSP00000476480.1:p.Tyr126Ter
ENST00000620705.4:c.393T>A ENSP00000484415.1:p.Tyr131Ter
NM_001002009.2:c.276T>A NP_001002009.1:p.Tyr92Ter
NM_001002010.2:c.393T>A NP_001002010.1:p.Tyr131Ter
NM_001166118.2:c.240T>A NP_001159590.1:p.Tyr80Ter
NM_016489.12:c.276T>A NP_057573.2:p.Tyr92Ter
XM_011515409.1:c.240T>A XP_011513711.1:p.Tyr80Ter
NM_001002010.3:c.378T>A NP_001002010.2:p.Tyr126Ter
NM_001356996.1:c.240T>A NP_001343925.1:p.Tyr80Ter
NM_001002009.3:c.276T>A NP_001002009.1:p.Tyr92Ter
NM_001002010.5:c.378T>A MANE Select NP_001002010.2:p.Tyr126Ter
NM_001166118.3:c.240T>A NP_001159590.1:p.Tyr80Ter
NM_001356996.2:c.240T>A NP_001343925.1:p.Tyr80Ter
NM_001374335.1:c.279T>A NP_001361264.1:p.Tyr93Ter
NM_001374336.1:c.240T>A NP_001361265.1:p.Tyr80Ter
NM_001374337.1:c.240T>A NP_001361266.1:p.Tyr80Ter
NM_001374338.1:c.378T>A NP_001361267.1:p.Tyr126Ter
NM_001374339.1:c.177T>A NP_001361268.1:p.Tyr59Ter
NM_016489.13:c.276T>A NP_057573.2:p.Tyr92Ter
NM_001356996.3:c.240T>A NP_001343925.1:p.Tyr80Ter
NM_016489.14:c.276T>A NP_057573.2:p.Tyr92Ter
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