Canonical Allele Identifier: CA2275552416

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75523986_75523988delinsCTT , CM000679.2:g.75523986_75523988delinsCTT	GRCh38
NC_000017.10:g.73520067_73520069delinsCTT , CM000679.1:g.73520067_73520069delinsCTT	GRCh37
NC_000017.9:g.71031662_71031664delinsCTT	NCBI36
NG_013041.1:g.12459_12461delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1430+207_1430+209delinsCTT MANE Select	ENSP00000327487.6:n.1430+207_1430+209delinsCTT
ENST00000434205.8:c.1127+207_1127+209delinsCTT	ENSP00000406559.4:n.1127+207_1127+209delinsCTT
ENST00000545228.3:c.1618+207_1618+209delinsCTT	ENSP00000438169.3:n.1618+207_1618+209delinsCTT
ENST00000577197.2:n.628+207_628+209delinsCTT
ENST00000579449.2:n.2170+207_2170+209delinsCTT
ENST00000580013.6:n.2574+207_2574+209delinsCTT
ENST00000679370.1:n.2952+207_2952+209delinsCTT
ENST00000679429.1:c.*888+207_*888+209delinsCTT	ENSP00000505403.1:n.*888+207_*888+209delinsCTT
ENST00000679443.1:n.1499+207_1499+209delinsCTT
ENST00000679782.1:c.*129+207_*129+209delinsCTT	ENSP00000505995.1:n.*129+207_*129+209delinsCTT
ENST00000679919.1:n.1701+207_1701+209delinsCTT
ENST00000679928.1:c.*1982+207_*1982+209delinsCTT	ENSP00000506071.1:n.*1982+207_*1982+209delinsCTT
ENST00000680528.1:n.2396+207_2396+209delinsCTT
ENST00000680999.1:c.1643+207_1643+209delinsCTT	ENSP00000504984.1:n.1643+207_1643+209delinsCTT
ENST00000681282.1:c.*1617+207_*1617+209delinsCTT	ENSP00000506339.1:n.*1617+207_*1617+209delinsCTT
ENST00000333213.10:c.1430+207_1430+209delinsCTT	ENSP00000327487.6:n.1430+207_1430+209delinsCTT
ENST00000545228.2:c.707+207_707+209delinsCTT
ENST00000577197.1:n.178+207_178+209delinsCTT
ENST00000579449.1:n.627+207_627+209delinsCTT
NM_207346.2:c.1430+207_1430+209delinsCTT	NP_997229.2:n.1430+207_1430+209delinsCTT
XM_005257229.2:c.1618+207_1618+209delinsCTT	XP_005257286.1:n.1618+207_1618+209delinsCTT
XM_006721821.2:c.1315+207_1315+209delinsCTT	XP_006721884.1:n.1315+207_1315+209delinsCTT
XM_011524616.1:c.1502-276_1502-274delinsCTT	XP_011522918.1:n.1502-276_1502-274delinsCTT
XM_011524617.1:c.*13-276_*13-274delinsCTT	XP_011522919.1:n.*13-276_*13-274delinsCTT
XM_011524618.1:c.1314-276_1314-274delinsCTT	XP_011522920.1:n.1314-276_1314-274delinsCTT
XR_243646.2:n.1662+207_1662+209delinsCTT
XM_005257229.4:c.1618+207_1618+209delinsCTT	XP_005257286.1:n.1618+207_1618+209delinsCTT
XR_001753015.1:n.87+323_87+325delinsAAG
XR_001753016.1:n.88+323_88+325delinsAAG
XR_243646.4:n.1668+207_1668+209delinsCTT
NM_207346.3:c.1430+207_1430+209delinsCTT MANE Select	NP_997229.2:n.1430+207_1430+209delinsCTT