Canonical Allele Identifier: CA2275548080
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516167T= , CM000679.2:g.75516167T= GRCh38
NC_000017.10:g.73512248T= , CM000679.1:g.73512248T= GRCh37
NC_000017.9:g.71023843T= NCBI36
NG_013041.1:g.4640T=
NG_033152.1:g.4417A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-302T= ENSP00000406559.4:n.-302T=
ENST00000679370.1:n.224T=
ENST00000434205.7:c.-302T= ENSP00000406559.3:n.-302T=
XM_006721821.2:c.-467T= XP_006721884.1:n.-467T=