Canonical Allele Identifier: CA2639833832
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516252A>G , CM000679.2:g.75516252A>G GRCh38
NC_000017.10:g.73512333A>G , CM000679.1:g.73512333A>G GRCh37
NC_000017.9:g.71023928A>G NCBI36
NG_013041.1:g.4725A>G
NG_033152.1:g.4332T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-217A>G ENSP00000406559.4:n.-217A>G
ENST00000679370.1:n.309A>G
ENST00000434205.7:c.-217A>G ENSP00000406559.3:n.-217A>G
XM_006721821.2:c.-382A>G XP_006721884.1:n.-382A>G