Canonical Allele Identifier: CA2275548088
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516175C= , CM000679.2:g.75516175C= GRCh38
NC_000017.10:g.73512256C= , CM000679.1:g.73512256C= GRCh37
NC_000017.9:g.71023851C= NCBI36
NG_013041.1:g.4648C=
NG_033152.1:g.4409G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-294C= ENSP00000406559.4:n.-294C=
ENST00000679370.1:n.232C=
ENST00000434205.7:c.-294C= ENSP00000406559.3:n.-294C=
XM_006721821.2:c.-459C= XP_006721884.1:n.-459C=