Canonical Allele Identifier: CA174224695

Gene: TRIM35

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27294279C>T , CM000670.2:g.27294279C>T	GRCh38
NC_000008.10:g.27151796C>T , CM000670.1:g.27151796C>T	GRCh37
NC_000008.9:g.27207713C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_171982.5:c.563G>A MANE Select	NP_741983.2:p.Arg188Gln
ENST00000305364.9:c.563G>A MANE Select	ENSP00000301924.4:p.Arg188Gln
NM_001304495.1:c.467G>A	NP_001291424.1:p.Arg156Gln
NM_001304495.2:c.467G>A	NP_001291424.1:p.Arg156Gln
NM_001362813.1:c.563G>A	NP_001349742.1:p.Arg188Gln
NM_001362813.2:c.563G>A	NP_001349742.1:p.Arg188Gln
NM_171982.4:c.563G>A	NP_741983.2:p.Arg188Gln
ENST00000305364.8:c.563G>A	ENSP00000301924.4:p.Arg188Gln
ENST00000519219.1:n.184G>A
ENST00000521253.1:c.467G>A	ENSP00000428770.1:p.Arg156Gln
XM_005273452.2:c.563G>A	XP_005273509.1:p.Arg188Gln
XM_011544453.1:c.113G>A	XP_011542755.1:p.Arg38Gln