Canonical Allele Identifier: CA363052338

Gene: TRIM31 TRIM31-AS1

Linked Data

• dbSNP Id: rs2023472
• gnomAD v2: 6-30075864-A-C
• gnomAD v4: 6-30108087-A-C
• MyVariant Identifiers: chr6:g.30075864A>C (hg19) ; chr6:g.30108087A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000376734.4:c.849T>G (TRIM31) MANE Select	ENSP00000365924.3:p.His283Gln
ENST00000376734.3:c.849T>G (TRIM31)	ENSP00000365924.3:p.His283Gln
ENST00000468264.1:n.113T>G (TRIM31)
ENST00000485864.5:n.539T>G (TRIM31)
NM_007028.3:c.849T>G (TRIM31)	NP_008959.3:p.His283Gln
NR_126470.1:n.273+300A>C (TRIM31-AS1)
XM_011514264.1:c.846T>G (TRIM31)	XP_011512566.1:p.His282Gln
XM_011514265.1:c.849T>G (TRIM31)	XP_011512567.1:p.His283Gln
XM_011514266.1:c.*82T>G (TRIM31)	XP_011512568.1:n.*82T>G
XR_926036.1:n.959T>G (TRIM31)
XR_926037.1:n.915T>G (TRIM31)
NM_007028.4:c.849T>G (TRIM31)	NP_008959.3:p.His283Gln
NR_134870.1:n.975T>G (TRIM31)
NR_134871.1:n.908T>G (TRIM31)
NM_007028.5:c.849T>G (TRIM31) MANE Select	NP_008959.3:p.His283Gln
NR_134870.2:n.959T>G (TRIM31)
NR_134871.2:n.892T>G (TRIM31)