Canonical Allele Identifier: CA2275552427

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524013_75524018delinsACTCAC , CM000679.2:g.75524013_75524018delinsACTCAC	GRCh38
NC_000017.10:g.73520094_73520099delinsACTCAC , CM000679.1:g.73520094_73520099delinsACTCAC	GRCh37
NC_000017.9:g.71031689_71031694delinsACTCAC	NCBI36
NG_013041.1:g.12486_12491delinsACTCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1430+234_1430+239delinsACTCAC MANE Select	ENSP00000327487.6:n.1430+234_1430+239delinsACTCAC
ENST00000434205.8:c.1127+234_1127+239delinsACTCAC	ENSP00000406559.4:n.1127+234_1127+239delinsACTCAC
ENST00000545228.3:c.1618+234_1618+239delinsACTCAC	ENSP00000438169.3:n.1618+234_1618+239delinsACTCAC
ENST00000577197.2:n.628+234_628+239delinsACTCAC
ENST00000579449.2:n.2170+234_2170+239delinsACTCAC
ENST00000580013.6:n.2574+234_2574+239delinsACTCAC
ENST00000679370.1:n.2952+234_2952+239delinsACTCAC
ENST00000679429.1:c.*888+234_*888+239delinsACTCAC	ENSP00000505403.1:n.*888+234_*888+239delinsACTCAC
ENST00000679443.1:n.1499+234_1499+239delinsACTCAC
ENST00000679782.1:c.*129+234_*129+239delinsACTCAC	ENSP00000505995.1:n.*129+234_*129+239delinsACTCAC
ENST00000679919.1:n.1701+234_1701+239delinsACTCAC
ENST00000679928.1:c.*1982+234_*1982+239delinsACTCAC	ENSP00000506071.1:n.*1982+234_*1982+239delinsACTCAC
ENST00000680528.1:n.2396+234_2396+239delinsACTCAC
ENST00000680999.1:c.1643+234_1643+239delinsACTCAC	ENSP00000504984.1:n.1643+234_1643+239delinsACTCAC
ENST00000681282.1:c.*1617+234_*1617+239delinsACTCAC	ENSP00000506339.1:n.*1617+234_*1617+239delinsACTCAC
ENST00000333213.10:c.1430+234_1430+239delinsACTCAC	ENSP00000327487.6:n.1430+234_1430+239delinsACTCAC
ENST00000545228.2:c.707+234_707+239delinsACTCAC
ENST00000577197.1:n.178+234_178+239delinsACTCAC
ENST00000579449.1:n.627+234_627+239delinsACTCAC
NM_207346.2:c.1430+234_1430+239delinsACTCAC	NP_997229.2:n.1430+234_1430+239delinsACTCAC
XM_005257229.2:c.1618+234_1618+239delinsACTCAC	XP_005257286.1:n.1618+234_1618+239delinsACTCAC
XM_006721821.2:c.1315+234_1315+239delinsACTCAC	XP_006721884.1:n.1315+234_1315+239delinsACTCAC
XM_011524616.1:c.1502-249_1502-244delinsACTCAC	XP_011522918.1:n.1502-249_1502-244delinsACTCAC
XM_011524617.1:c.*13-249_*13-244delinsACTCAC	XP_011522919.1:n.*13-249_*13-244delinsACTCAC
XM_011524618.1:c.1314-249_1314-244delinsACTCAC	XP_011522920.1:n.1314-249_1314-244delinsACTCAC
XR_243646.2:n.1662+234_1662+239delinsACTCAC
XM_005257229.4:c.1618+234_1618+239delinsACTCAC	XP_005257286.1:n.1618+234_1618+239delinsACTCAC
XR_001753015.1:n.87+293_87+298delinsGTGAGT
XR_001753016.1:n.88+293_88+298delinsGTGAGT
XR_243646.4:n.1668+234_1668+239delinsACTCAC
NM_207346.3:c.1430+234_1430+239delinsACTCAC MANE Select	NP_997229.2:n.1430+234_1430+239delinsACTCAC