Canonical Allele Identifier: CA2639836380
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75524538G>A , CM000679.2:g.75524538G>A GRCh38
NC_000017.10:g.73520619G>A , CM000679.1:g.73520619G>A GRCh37
NC_000017.9:g.71032214G>A NCBI36
NG_013041.1:g.13011G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333213.11:c.*126G>A MANE Select ENSP00000327487.6:n.*126G>A
ENST00000434205.8:c.*126G>A ENSP00000406559.4:n.*126G>A
ENST00000545228.3:c.*206G>A ENSP00000438169.3:n.*206G>A
ENST00000577197.2:n.905G>A
ENST00000579449.2:n.2447G>A
ENST00000580013.6:n.2851G>A
ENST00000679370.1:n.3229G>A
ENST00000679429.1:c.*1165G>A ENSP00000505403.1:n.*1165G>A
ENST00000679443.1:n.1776G>A
ENST00000679782.1:c.*406G>A ENSP00000505995.1:n.*406G>A
ENST00000679919.1:n.1978G>A
ENST00000679928.1:c.*2259G>A ENSP00000506071.1:n.*2259G>A
ENST00000680999.1:c.*126G>A ENSP00000504984.1:n.*126G>A
ENST00000681282.1:c.*1894G>A ENSP00000506339.1:n.*1894G>A
ENST00000333213.10:c.*126G>A ENSP00000327487.6:n.*126G>A
ENST00000545228.2:c.984G>A
ENST00000577197.1:n.455G>A
NM_207346.2:c.*126G>A NP_997229.2:n.*126G>A
XM_005257229.2:c.*206G>A XP_005257286.1:n.*206G>A
XM_006721821.2:c.*206G>A XP_006721884.1:n.*206G>A
XM_011524616.1:c.*206G>A XP_011522918.1:n.*206G>A
XM_011524618.1:c.*126G>A XP_011522920.1:n.*126G>A
XR_243646.2:n.1939G>A
XM_005257229.4:c.*206G>A XP_005257286.1:n.*206G>A
XR_243646.4:n.1945G>A
NM_207346.3:c.*126G>A MANE Select NP_997229.2:n.*126G>A