Canonical Allele Identifier: CA4687710

Gene: TRIM35

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27287819C>T , CM000670.2:g.27287819C>T	GRCh38
NC_000008.10:g.27145336C>T , CM000670.1:g.27145336C>T	GRCh37
NC_000008.9:g.27201253C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_171982.5:c.1213G>A MANE Select	NP_741983.2:p.Val405Met
ENST00000305364.9:c.1213G>A MANE Select	ENSP00000301924.4:p.Val405Met
NM_001304495.1:c.*293G>A	NP_001291424.1:n.*293G>A
NM_001304495.2:c.*293G>A	NP_001291424.1:n.*293G>A
NM_001362813.1:c.*293G>A	NP_001349742.1:n.*293G>A
NM_001362813.2:c.*293G>A	NP_001349742.1:n.*293G>A
NM_171982.4:c.1213G>A	NP_741983.2:p.Val405Met
ENST00000305364.8:c.1213G>A	ENSP00000301924.4:p.Val405Met
ENST00000521253.1:c.*293G>A	ENSP00000428770.1:n.*293G>A
ENST00000521283.1:c.290+217G>A
XM_005273452.2:c.*293G>A	XP_005273509.1:n.*293G>A
XM_011544453.1:c.763G>A	XP_011542755.1:p.Val255Met