Canonical Allele Identifier: CA2275548063
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516132G= , CM000679.2:g.75516132G= GRCh38
NC_000017.10:g.73512213G= , CM000679.1:g.73512213G= GRCh37
NC_000017.9:g.71023808G= NCBI36
NG_013041.1:g.4605G=
NG_033152.1:g.4452C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-337G= ENSP00000406559.4:n.-337G=
ENST00000679370.1:n.189G=
ENST00000434205.7:c.-337G= ENSP00000406559.3:n.-337G=
XM_006721821.2:c.-502G= XP_006721884.1:n.-502G=