Canonical Allele Identifier: CA2275548132
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516259G= , CM000679.2:g.75516259G= GRCh38
NC_000017.10:g.73512340G= , CM000679.1:g.73512340G= GRCh37
NC_000017.9:g.71023935G= NCBI36
NG_013041.1:g.4732G=
NG_033152.1:g.4325C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-210G= ENSP00000406559.4:n.-210G=
ENST00000679370.1:n.316G=
ENST00000434205.7:c.-210G= ENSP00000406559.3:n.-210G=
XM_006721821.2:c.-375G= XP_006721884.1:n.-375G=