Canonical Allele Identifier: CA2275548163
Gene: TSEN54 HGNC NCBI

Linked Data

dbSNP Id: rs2053363768

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516320G>A , CM000679.2:g.75516320G>A GRCh38
NC_000017.10:g.73512401G>A , CM000679.1:g.73512401G>A GRCh37
NC_000017.9:g.71023996G>A NCBI36
NG_013041.1:g.4793G>A
NG_033152.1:g.4264C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-149G>A ENSP00000406559.4:n.-149G>A
ENST00000679370.1:n.377G>A
ENST00000434205.7:c.-149G>A ENSP00000406559.3:n.-149G>A
XM_006721821.2:c.-314G>A XP_006721884.1:n.-314G>A