Canonical Allele Identifier: CA84615166
Gene: TRIM42 HGNC NCBI

Linked Data

dbSNP Id: rs79436609

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.140698604T>C , CM000665.2:g.140698604T>C GRCh38
NC_000003.11:g.140417446T>C , CM000665.1:g.140417446T>C GRCh37
NC_000003.10:g.141900136T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000286349.4:c.2086-2284T>C MANE Select ENSP00000286349.3:n.2086-2284T>C
ENST00000286349.3:c.2086-2284T>C ENSP00000286349.3:n.2086-2284T>C
NM_152616.4:c.2086-2284T>C NP_689829.3:n.2086-2284T>C
XM_011512740.1:c.2086-1812T>C XP_011511042.1:n.2086-1812T>C
XM_011512741.1:c.1645-1812T>C XP_011511043.1:n.1645-1812T>C
XM_011512740.3:c.2086-1812T>C XP_011511042.1:n.2086-1812T>C
XR_001740121.2:n.2339+2095T>C
XR_001740122.2:n.2340-1812T>C
NM_152616.5:c.2086-2284T>C MANE Select NP_689829.3:n.2086-2284T>C