Canonical Allele Identifier: CA1618592360

Gene: TRIM31 TRIM31-AS1

Genomic Alleles

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

Transcript Alleles

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