Canonical Allele Identifier: CA2275548079
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516165C= , CM000679.2:g.75516165C= GRCh38
NC_000017.10:g.73512246C= , CM000679.1:g.73512246C= GRCh37
NC_000017.9:g.71023841C= NCBI36
NG_013041.1:g.4638C=
NG_033152.1:g.4419G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-304C= ENSP00000406559.4:n.-304C=
ENST00000679370.1:n.222C=
ENST00000434205.7:c.-304C= ENSP00000406559.3:n.-304C=
XM_006721821.2:c.-469C= XP_006721884.1:n.-469C=