Canonical Allele Identifier: CA2275548091
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516177C= , CM000679.2:g.75516177C= GRCh38
NC_000017.10:g.73512258C= , CM000679.1:g.73512258C= GRCh37
NC_000017.9:g.71023853C= NCBI36
NG_013041.1:g.4650C=
NG_033152.1:g.4407G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-292C= ENSP00000406559.4:n.-292C=
ENST00000679370.1:n.234C=
ENST00000434205.7:c.-292C= ENSP00000406559.3:n.-292C=
XM_006721821.2:c.-457C= XP_006721884.1:n.-457C=