Canonical Allele Identifier: CA2830535499

Gene: TRIM42

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.140678741G>T , CM000665.2:g.140678741G>T	GRCh38
NC_000003.11:g.140397583G>T , CM000665.1:g.140397583G>T	GRCh37
NC_000003.10:g.141880273G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286349.4:c.341+171G>T MANE Select	ENSP00000286349.3:n.341+171G>T
ENST00000286349.3:c.341+171G>T	ENSP00000286349.3:n.341+171G>T
NM_152616.4:c.341+171G>T	NP_689829.3:n.341+171G>T
XM_011512740.1:c.341+171G>T	XP_011511042.1:n.341+171G>T
XM_011512741.1:c.-221+171G>T	XP_011511043.1:n.-221+171G>T
XM_011512740.3:c.341+171G>T	XP_011511042.1:n.341+171G>T
XR_001740121.2:n.518+171G>T
XR_001740122.2:n.518+171G>T
NM_152616.5:c.341+171G>T MANE Select	NP_689829.3:n.341+171G>T