Canonical Allele Identifier: CA2682336289
Gene: NT5C3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.33021244dup , CM000669.2:g.33021244dup GRCh38
NC_000007.13:g.33060856dup , CM000669.1:g.33060856dup GRCh37
NC_000007.12:g.33027381dup NCBI36
NG_015800.1:g.46555dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000409467.6:c.302+29dup ENSP00000387166.1:n.302+29dup
ENST00000610140.7:c.440+29dup MANE Select ENSP00000476480.2:n.440+29dup
ENST00000643244.1:c.338+29dup ENSP00000496364.1:n.338+29dup
ENST00000242210.11:c.455+29dup ENSP00000242210.7:n.455+29dup
ENST00000381626.6:c.302+29dup ENSP00000371039.2:n.302+29dup
ENST00000396152.6:c.338+29dup ENSP00000379456.2:n.338+29dup
ENST00000405342.5:c.338+29dup ENSP00000385261.1:n.338+29dup
ENST00000409467.5:c.302+29dup ENSP00000387166.1:n.302+29dup
ENST00000409787.4:c.338+29dup ENSP00000387205.1:n.338+29dup
ENST00000456458.5:c.*345+29dup ENSP00000389676.2:n.*345+29dup
ENST00000610140.5:c.440+29dup ENSP00000476480.1:n.440+29dup
ENST00000620705.4:c.455+29dup ENSP00000484415.1:n.455+29dup
NM_001002009.2:c.338+29dup NP_001002009.1:n.338+29dup
NM_001002010.2:c.455+29dup NP_001002010.1:n.455+29dup
NM_001166118.2:c.302+29dup NP_001159590.1:n.302+29dup
NM_016489.12:c.338+29dup NP_057573.2:n.338+29dup
XM_011515409.1:c.302+29dup XP_011513711.1:n.302+29dup
NM_001002010.3:c.440+29dup NP_001002010.2:n.440+29dup
NM_001356996.1:c.302+29dup NP_001343925.1:n.302+29dup
NM_001002009.3:c.338+29dup NP_001002009.1:n.338+29dup
NM_001002010.5:c.440+29dup MANE Select NP_001002010.2:n.440+29dup
NM_001166118.3:c.302+29dup NP_001159590.1:n.302+29dup
NM_001356996.2:c.302+29dup NP_001343925.1:n.302+29dup
NM_001374335.1:c.341+29dup NP_001361264.1:n.341+29dup
NM_001374336.1:c.302+29dup NP_001361265.1:n.302+29dup
NM_001374337.1:c.302+29dup NP_001361266.1:n.302+29dup
NM_001374338.1:c.440+29dup NP_001361267.1:n.440+29dup
NM_001374339.1:c.239+29dup NP_001361268.1:n.239+29dup
NM_016489.13:c.338+29dup NP_057573.2:n.338+29dup
NM_001356996.3:c.302+29dup NP_001343925.1:n.302+29dup
NM_016489.14:c.338+29dup NP_057573.2:n.338+29dup