Canonical Allele Identifier: CA2275552727

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524632_75524664delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC , CM000679.2:g.75524632_75524664delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC	GRCh38
NC_000017.10:g.73520713_73520745delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC , CM000679.1:g.73520713_73520745delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC	GRCh37
NC_000017.9:g.71032308_71032340delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC	NCBI36
NG_013041.1:g.13105_13137delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*220_*252delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC MANE Select	ENSP00000327487.6:n.*220_*252delinsTAAGGACCCAGGAGGTGGGGCAGAAG...
ENST00000434205.8:c.*220_*252delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC	ENSP00000406559.4:n.*220_*252delinsTAAGGACCCAGGAGGTGGGGCAGAAG...
ENST00000545228.3:c.*300_*332delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC	ENSP00000438169.3:n.*300_*332delinsTAAGGACCCAGGAGGTGGGGCAGAAG...
ENST00000577197.2:n.999_1031delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC
ENST00000579449.2:n.2541_2573delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC
ENST00000580013.6:n.2945_2977delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC
ENST00000679370.1:n.3323_3355delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC
ENST00000679429.1:c.*1259_*1291delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC	ENSP00000505403.1:n.*1259_*1291delinsTAAGGACCCAGGAGGTGGGGCAGA...
ENST00000679443.1:n.1870_1902delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC
ENST00000679782.1:c.*500_*532delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC	ENSP00000505995.1:n.*500_*532delinsTAAGGACCCAGGAGGTGGGGCAGAAG...
ENST00000679919.1:n.2072_2104delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC
ENST00000679928.1:c.*2353_*2385delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC	ENSP00000506071.1:n.*2353_*2385delinsTAAGGACCCAGGAGGTGGGGCAGA...
ENST00000680999.1:c.*220_*252delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC	ENSP00000504984.1:n.*220_*252delinsTAAGGACCCAGGAGGTGGGGCAGAAG...
ENST00000681282.1:c.*1988_*2020delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC	ENSP00000506339.1:n.*1988_*2020delinsTAAGGACCCAGGAGGTGGGGCAGA...
ENST00000333213.10:c.*220_*252delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC	ENSP00000327487.6:n.*220_*252delinsTAAGGACCCAGGAGGTGGGGCAGAAG...
ENST00000545228.2:c.1078_1110delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC
ENST00000577197.1:n.549_581delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC
NM_207346.2:c.*220_*252delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC	NP_997229.2:n.*220_*252delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGA...
XM_005257229.2:c.*300_*332delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC	XP_005257286.1:n.*300_*332delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGA...
XM_006721821.2:c.*300_*332delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC	XP_006721884.1:n.*300_*332delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGA...
XM_011524616.1:c.*300_*332delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC	XP_011522918.1:n.*300_*332delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGA...
XM_011524618.1:c.*220_*252delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC	XP_011522920.1:n.*220_*252delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGA...
XR_243646.2:n.2033_2065delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC
XM_005257229.4:c.*300_*332delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC	XP_005257286.1:n.*300_*332delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGA...
XR_243646.4:n.2039_2071delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC
NM_207346.3:c.*220_*252delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGAC MANE Select	NP_997229.2:n.*220_*252delinsTAAGGACCCAGGAGGTGGGGCAGAAGAGAGGA...