Canonical Allele Identifier: CA3694870
Gene: TRIM31 HGNC NCBI
TRIM31-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30112592G>T , CM000668.2:g.30112592G>T GRCh38
NC_000006.11:g.30080369G>T , CM000668.1:g.30080369G>T GRCh37
NC_000006.10:g.30188348G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376734.4:c.214C>A (TRIM31) MANE Select ENSP00000365924.3:p.Arg72=
ENST00000376734.3:c.214C>A (TRIM31) ENSP00000365924.3:p.Arg72=
NM_007028.3:c.214C>A (TRIM31) NP_008959.3:p.Arg72=
NR_126470.1:n.395+753G>T (TRIM31-AS1)
XM_011514264.1:c.214C>A (TRIM31) XP_011512566.1:p.Arg72=
XM_011514265.1:c.214C>A (TRIM31) XP_011512567.1:p.Arg72=
XM_011514266.1:c.214C>A (TRIM31) XP_011512568.1:p.Arg72=
XR_926036.1:n.324C>A (TRIM31)
XR_926037.1:n.324C>A (TRIM31)
NM_007028.4:c.214C>A (TRIM31) NP_008959.3:p.Arg72=
NR_134870.1:n.340C>A (TRIM31)
NR_134871.1:n.340C>A (TRIM31)
NM_007028.5:c.214C>A (TRIM31) MANE Select NP_008959.3:p.Arg72=
NR_134870.2:n.324C>A (TRIM31)
NR_134871.2:n.324C>A (TRIM31)
Search 100 bp 5'
Search 100 bp 3'