Canonical Allele Identifier: CA2639835107
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516484_75516485insA , CM000679.2:g.75516484_75516485insA GRCh38
NC_000017.10:g.73512565_73512566insA , CM000679.1:g.73512565_73512566insA GRCh37
NC_000017.9:g.71024160_71024161insA NCBI36
NG_013041.1:g.4957_4958insA
NG_033152.1:g.4099_4100insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-83+98_-83+99insA ENSP00000406559.4:n.-83+98_-83+99insA
ENST00000679370.1:n.443+98_443+99insA
ENST00000434205.7:c.-83+98_-83+99insA ENSP00000406559.3:n.-83+98_-83+99insA
XM_006721821.2:c.-248+98_-248+99insA XP_006721884.1:n.-248+98_-248+99insA