Canonical Allele Identifier: CA2639833757
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516229_75516230insT , CM000679.2:g.75516229_75516230insT GRCh38
NC_000017.10:g.73512310_73512311insT , CM000679.1:g.73512310_73512311insT GRCh37
NC_000017.9:g.71023905_71023906insT NCBI36
NG_013041.1:g.4702_4703insT
NG_033152.1:g.4354_4355insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-240_-239insT ENSP00000406559.4:n.-240_-239insT
ENST00000679370.1:n.286_287insT
ENST00000434205.7:c.-240_-239insT ENSP00000406559.3:n.-240_-239insT
XM_006721821.2:c.-405_-404insT XP_006721884.1:n.-405_-404insT