Canonical Allele Identifier: CA2275548066
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516147G= , CM000679.2:g.75516147G= GRCh38
NC_000017.10:g.73512228G= , CM000679.1:g.73512228G= GRCh37
NC_000017.9:g.71023823G= NCBI36
NG_013041.1:g.4620G=
NG_033152.1:g.4437C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-322G= ENSP00000406559.4:n.-322G=
ENST00000679370.1:n.204G=
ENST00000434205.7:c.-322G= ENSP00000406559.3:n.-322G=
XM_006721821.2:c.-487G= XP_006721884.1:n.-487G=