Canonical Allele Identifier: CA2639833783
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516242_75516243insCTGTC , CM000679.2:g.75516242_75516243insCTGTC GRCh38
NC_000017.10:g.73512323_73512324insCTGTC , CM000679.1:g.73512323_73512324insCTGTC GRCh37
NC_000017.9:g.71023918_71023919insCTGTC NCBI36
NG_013041.1:g.4715_4716insCTGTC
NG_033152.1:g.4344_4345insAGGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-227_-226insCTGTC ENSP00000406559.4:n.-227_-226insCTGTC
ENST00000679370.1:n.299_300insCTGTC
ENST00000434205.7:c.-227_-226insCTGTC ENSP00000406559.3:n.-227_-226insCTGTC
XM_006721821.2:c.-392_-391insCTGTC XP_006721884.1:n.-392_-391insCTGTC