Canonical Allele Identifier: CA4687750
Community Standard Title: NM_171982.5(TRIM35):c.1064C>T (p.Ser355Leu)
Gene: TRIM35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27287968G>A , CM000670.2:g.27287968G>A GRCh38
NC_000008.10:g.27145485G>A , CM000670.1:g.27145485G>A GRCh37
NC_000008.9:g.27201402G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_171982.5:c.1064C>T MANE Select NP_741983.2:p.Ser355Leu
ENST00000305364.9:c.1064C>T MANE Select ENSP00000301924.4:p.Ser355Leu
NM_001304495.1:c.*144C>T NP_001291424.1:n.*144C>T
NM_001304495.2:c.*144C>T NP_001291424.1:n.*144C>T
NM_001362813.1:c.*144C>T NP_001349742.1:n.*144C>T
NM_001362813.2:c.*144C>T NP_001349742.1:n.*144C>T
NM_171982.4:c.1064C>T NP_741983.2:p.Ser355Leu
ENST00000305364.8:c.1064C>T ENSP00000301924.4:p.Ser355Leu
ENST00000521253.1:c.*144C>T ENSP00000428770.1:n.*144C>T
ENST00000521283.1:c.290+68C>T
XM_005273452.2:c.*144C>T XP_005273509.1:n.*144C>T
XM_011544453.1:c.614C>T XP_011542755.1:p.Ser205Leu