Canonical Allele Identifier: CA2275548057
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516116G= , CM000679.2:g.75516116G= GRCh38
NC_000017.10:g.73512197G= , CM000679.1:g.73512197G= GRCh37
NC_000017.9:g.71023792G= NCBI36
NG_013041.1:g.4589G=
NG_033152.1:g.4468C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-353G= ENSP00000406559.4:n.-353G=
ENST00000679370.1:n.173G=
ENST00000434205.7:c.-353G= ENSP00000406559.3:n.-353G=
XM_006721821.2:c.-518G= XP_006721884.1:n.-518G=