Canonical Allele Identifier: CA3694671
Gene: TRIM31 HGNC NCBI
TRIM31-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2023472
gnomAD v2: 6-30075864-A-G
gnomAD v3: 6-30108087-A-G
gnomAD v4: 6-30108087-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30108087A>G , CM000668.2:g.30108087A>G GRCh38
NC_000006.11:g.30075864A>G , CM000668.1:g.30075864A>G GRCh37
NC_000006.10:g.30183843A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376734.4:c.849T>C (TRIM31) MANE Select ENSP00000365924.3:p.His283=
ENST00000376734.3:c.849T>C (TRIM31) ENSP00000365924.3:p.His283=
ENST00000468264.1:n.113T>C (TRIM31)
ENST00000485864.5:n.539T>C (TRIM31)
NM_007028.3:c.849T>C (TRIM31) NP_008959.3:p.His283=
NR_126470.1:n.273+300A>G (TRIM31-AS1)
XM_011514264.1:c.846T>C (TRIM31) XP_011512566.1:p.His282=
XM_011514265.1:c.849T>C (TRIM31) XP_011512567.1:p.His283=
XM_011514266.1:c.*82T>C (TRIM31) XP_011512568.1:n.*82T>C
XR_926036.1:n.959T>C (TRIM31)
XR_926037.1:n.915T>C (TRIM31)
NM_007028.4:c.849T>C (TRIM31) NP_008959.3:p.His283=
NR_134870.1:n.975T>C (TRIM31)
NR_134871.1:n.908T>C (TRIM31)
NM_007028.5:c.849T>C (TRIM31) MANE Select NP_008959.3:p.His283=
NR_134870.2:n.959T>C (TRIM31)
NR_134871.2:n.892T>C (TRIM31)