Canonical Allele Identifier: CA2275548455

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516764_75516787delinsCGCCCGCTCGCGGTCGCAGAAGCT , CM000679.2:g.75516764_75516787delinsCGCCCGCTCGCGGTCGCAGAAGCT	GRCh38
NC_000017.10:g.73512845_73512868delinsCGCCCGCTCGCGGTCGCAGAAGCT , CM000679.1:g.73512845_73512868delinsCGCCCGCTCGCGGTCGCAGAAGCT	GRCh37
NC_000017.9:g.71024440_71024463delinsCGCCCGCTCGCGGTCGCAGAAGCT	NCBI36
NG_013041.1:g.5237_5260delinsCGCCCGCTCGCGGTCGCAGAAGCT
NG_033152.1:g.3797_3820delinsAGCTTCTGCGACCGCGAGCGGGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.75_98delinsCGCCCGCTCGCGGTCGCAGAAGCT MANE Select	ENSP00000327487.6:p.Ala25=
ENST00000434205.8:c.-82-245_-82-222delinsCGCCCGCTCGCGGTCGCAGAAGCT	ENSP00000406559.4:n.-82-245_-82-222delinsCGCCCGCTCGCGGTCGCAGA...
ENST00000545228.3:c.75_98delinsCGCCCGCTCGCGGTCGCAGAAGCT	ENSP00000438169.3:p.Ala25=
ENST00000579449.2:n.20+148_20+171delinsCGCCCGCTCGCGGTCGCAGAAGCT
ENST00000580013.6:n.84_107delinsCGCCCGCTCGCGGTCGCAGAAGCT
ENST00000583818.2:c.75_98delinsCGCCCGCTCGCGGTCGCAGAAGCT	ENSP00000461928.2:p.Ala25=
ENST00000679370.1:n.462_485delinsCGCCCGCTCGCGGTCGCAGAAGCT
ENST00000679429.1:c.75_98delinsCGCCCGCTCGCGGTCGCAGAAGCT	ENSP00000505403.1:p.Ala25=
ENST00000679782.1:c.75_98delinsCGCCCGCTCGCGGTCGCAGAAGCT	ENSP00000505995.1:p.Ala25=
ENST00000679928.1:c.75_98delinsCGCCCGCTCGCGGTCGCAGAAGCT	ENSP00000506071.1:p.Ala25=
ENST00000680528.1:n.100_123delinsCGCCCGCTCGCGGTCGCAGAAGCT
ENST00000680999.1:c.75_98delinsCGCCCGCTCGCGGTCGCAGAAGCT	ENSP00000504984.1:p.Ala25=
ENST00000681282.1:c.75_98delinsCGCCCGCTCGCGGTCGCAGAAGCT	ENSP00000506339.1:p.Ala25=
ENST00000333213.10:c.75_98delinsCGCCCGCTCGCGGTCGCAGAAGCT	ENSP00000327487.6:p.Ala25=
ENST00000434205.7:c.-82-245_-82-222delinsCGCCCGCTCGCGGTCGCAGAAGCT	ENSP00000406559.3:n.-82-245_-82-222delinsCGCCCGCTCGCGGTCGCAGA...
ENST00000580013.5:n.100_123delinsCGCCCGCTCGCGGTCGCAGAAGCT
ENST00000583173.5:c.56+148_56+171delinsCGCCCGCTCGCGGTCGCAGAAGCT	ENSP00000463619.1:n.56+148_56+171delinsCGCCCGCTCGCGGTCGCAGAAG...
ENST00000583454.1:n.110_133delinsCGCCCGCTCGCGGTCGCAGAAGCT
NM_207346.2:c.75_98delinsCGCCCGCTCGCGGTCGCAGAAGCT	NP_997229.2:p.Ala25=
XM_005257229.2:c.75_98delinsCGCCCGCTCGCGGTCGCAGAAGCT	XP_005257286.1:p.Ala25=
XM_006721821.2:c.-229_-206delinsCGCCCGCTCGCGGTCGCAGAAGCT	XP_006721884.1:n.-229_-206delinsCGCCCGCTCGCGGTCGCAGAAGCT
XM_011524616.1:c.75_98delinsCGCCCGCTCGCGGTCGCAGAAGCT	XP_011522918.1:p.Ala25=
XM_011524617.1:c.75_98delinsCGCCCGCTCGCGGTCGCAGAAGCT	XP_011522919.1:p.Ala25=
XM_011524618.1:c.75_98delinsCGCCCGCTCGCGGTCGCAGAAGCT	XP_011522920.1:p.Ala25=
XR_243646.2:n.105_128delinsCGCCCGCTCGCGGTCGCAGAAGCT
XM_005257229.4:c.75_98delinsCGCCCGCTCGCGGTCGCAGAAGCT	XP_005257286.1:p.Ala25=
XR_243646.4:n.111_134delinsCGCCCGCTCGCGGTCGCAGAAGCT
NM_207346.3:c.75_98delinsCGCCCGCTCGCGGTCGCAGAAGCT MANE Select	NP_997229.2:p.Ala25=