Canonical Allele Identifier: CA2639833432
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516090T>A , CM000679.2:g.75516090T>A GRCh38
NC_000017.10:g.73512171T>A , CM000679.1:g.73512171T>A GRCh37
NC_000017.9:g.71023766T>A NCBI36
NG_013041.1:g.4563T>A
NG_033152.1:g.4494A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-379T>A ENSP00000406559.4:n.-379T>A
ENST00000679370.1:n.147T>A
ENST00000434205.7:c.-379T>A ENSP00000406559.3:n.-379T>A
XM_006721821.2:c.-544T>A XP_006721884.1:n.-544T>A