Canonical Allele Identifier: CA2639833574
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516177_75516181del , CM000679.2:g.75516177_75516181del GRCh38
NC_000017.10:g.73512258_73512262del , CM000679.1:g.73512258_73512262del GRCh37
NC_000017.9:g.71023853_71023857del NCBI36
NG_013041.1:g.4650_4654del
NG_033152.1:g.4403_4407del

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-292_-288del ENSP00000406559.4:n.-292_-288del
ENST00000679370.1:n.234_238del
ENST00000434205.7:c.-292_-288del ENSP00000406559.3:n.-292_-288del
XM_006721821.2:c.-457_-453del XP_006721884.1:n.-457_-453del