Canonical Allele Identifier: CA2275548119
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516238C= , CM000679.2:g.75516238C= GRCh38
NC_000017.10:g.73512319C= , CM000679.1:g.73512319C= GRCh37
NC_000017.9:g.71023914C= NCBI36
NG_013041.1:g.4711C=
NG_033152.1:g.4346G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-231C= ENSP00000406559.4:n.-231C=
ENST00000679370.1:n.295C=
ENST00000434205.7:c.-231C= ENSP00000406559.3:n.-231C=
XM_006721821.2:c.-396C= XP_006721884.1:n.-396C=