Canonical Allele Identifier: CA2639834078
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516284T>C , CM000679.2:g.75516284T>C GRCh38
NC_000017.10:g.73512365T>C , CM000679.1:g.73512365T>C GRCh37
NC_000017.9:g.71023960T>C NCBI36
NG_013041.1:g.4757T>C
NG_033152.1:g.4300A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-185T>C ENSP00000406559.4:n.-185T>C
ENST00000679370.1:n.341T>C
ENST00000434205.7:c.-185T>C ENSP00000406559.3:n.-185T>C
XM_006721821.2:c.-350T>C XP_006721884.1:n.-350T>C