Canonical Allele Identifier: CA2639833652
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516205_75516206insAG , CM000679.2:g.75516205_75516206insAG GRCh38
NC_000017.10:g.73512286_73512287insAG , CM000679.1:g.73512286_73512287insAG GRCh37
NC_000017.9:g.71023881_71023882insAG NCBI36
NG_013041.1:g.4678_4679insAG
NG_033152.1:g.4379_4380insTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-264_-263insAG ENSP00000406559.4:n.-264_-263insAG
ENST00000679370.1:n.262_263insAG
ENST00000434205.7:c.-264_-263insAG ENSP00000406559.3:n.-264_-263insAG
XM_006721821.2:c.-429_-428insAG XP_006721884.1:n.-429_-428insAG