Canonical Allele Identifier: CA2275548112
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516226_75516228delinsGCT , CM000679.2:g.75516226_75516228delinsGCT GRCh38
NC_000017.10:g.73512307_73512309delinsGCT , CM000679.1:g.73512307_73512309delinsGCT GRCh37
NC_000017.9:g.71023902_71023904delinsGCT NCBI36
NG_013041.1:g.4699_4701delinsGCT
NG_033152.1:g.4356_4358delinsAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-243_-241delinsGCT ENSP00000406559.4:n.-243_-241delinsGCT
ENST00000679370.1:n.283_285delinsGCT
ENST00000434205.7:c.-243_-241delinsGCT ENSP00000406559.3:n.-243_-241delinsGCT
XM_006721821.2:c.-408_-406delinsGCT XP_006721884.1:n.-408_-406delinsGCT