Canonical Allele Identifier: CA2275548111
Gene: TSEN54 HGNC NCBI

Linked Data

dbSNP Id: rs1598472800

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516225G>A , CM000679.2:g.75516225G>A GRCh38
NC_000017.10:g.73512306G>A , CM000679.1:g.73512306G>A GRCh37
NC_000017.9:g.71023901G>A NCBI36
NG_013041.1:g.4698G>A
NG_033152.1:g.4359C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-244G>A ENSP00000406559.4:n.-244G>A
ENST00000679370.1:n.282G>A
ENST00000434205.7:c.-244G>A ENSP00000406559.3:n.-244G>A
XM_006721821.2:c.-409G>A XP_006721884.1:n.-409G>A