Canonical Allele Identifier: CA2275548137
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516273A= , CM000679.2:g.75516273A= GRCh38
NC_000017.10:g.73512354A= , CM000679.1:g.73512354A= GRCh37
NC_000017.9:g.71023949A= NCBI36
NG_013041.1:g.4746A=
NG_033152.1:g.4311T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-196A= ENSP00000406559.4:n.-196A=
ENST00000679370.1:n.330A=
ENST00000434205.7:c.-196A= ENSP00000406559.3:n.-196A=
XM_006721821.2:c.-361A= XP_006721884.1:n.-361A=