Canonical Allele Identifier: CA2639833523
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516140G>A , CM000679.2:g.75516140G>A GRCh38
NC_000017.10:g.73512221G>A , CM000679.1:g.73512221G>A GRCh37
NC_000017.9:g.71023816G>A NCBI36
NG_013041.1:g.4613G>A
NG_033152.1:g.4444C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-329G>A ENSP00000406559.4:n.-329G>A
ENST00000679370.1:n.197G>A
ENST00000434205.7:c.-329G>A ENSP00000406559.3:n.-329G>A
XM_006721821.2:c.-494G>A XP_006721884.1:n.-494G>A