Canonical Allele Identifier: CA2639834689
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516407T>G , CM000679.2:g.75516407T>G GRCh38
NC_000017.10:g.73512488T>G , CM000679.1:g.73512488T>G GRCh37
NC_000017.9:g.71024083T>G NCBI36
NG_013041.1:g.4880T>G
NG_033152.1:g.4177A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-83+21T>G ENSP00000406559.4:n.-83+21T>G
ENST00000679370.1:n.443+21T>G
ENST00000434205.7:c.-83+21T>G ENSP00000406559.3:n.-83+21T>G
XM_006721821.2:c.-248+21T>G XP_006721884.1:n.-248+21T>G