Canonical Allele Identifier: CA2275552472

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524113_75524116delinsCTCT , CM000679.2:g.75524113_75524116delinsCTCT	GRCh38
NC_000017.10:g.73520194_73520197delinsCTCT , CM000679.1:g.73520194_73520197delinsCTCT	GRCh37
NC_000017.9:g.71031789_71031792delinsCTCT	NCBI36
NG_013041.1:g.12586_12589delinsCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1431-149_1431-146delinsCTCT MANE Select	ENSP00000327487.6:n.1431-149_1431-146delinsCTCT
ENST00000434205.8:c.1128-149_1128-146delinsCTCT	ENSP00000406559.4:n.1128-149_1128-146delinsCTCT
ENST00000545228.3:c.1619-149_1619-146delinsCTCT	ENSP00000438169.3:n.1619-149_1619-146delinsCTCT
ENST00000577197.2:n.629-149_629-146delinsCTCT
ENST00000579449.2:n.2171-149_2171-146delinsCTCT
ENST00000580013.6:n.2575-149_2575-146delinsCTCT
ENST00000679370.1:n.2953-149_2953-146delinsCTCT
ENST00000679429.1:c.*889-149_*889-146delinsCTCT	ENSP00000505403.1:n.*889-149_*889-146delinsCTCT
ENST00000679443.1:n.1500-149_1500-146delinsCTCT
ENST00000679782.1:c.*130-149_*130-146delinsCTCT	ENSP00000505995.1:n.*130-149_*130-146delinsCTCT
ENST00000679919.1:n.1702-149_1702-146delinsCTCT
ENST00000679928.1:c.*1983-149_*1983-146delinsCTCT	ENSP00000506071.1:n.*1983-149_*1983-146delinsCTCT
ENST00000680528.1:n.2397-149_2397-146delinsCTCT
ENST00000680999.1:c.1644-149_1644-146delinsCTCT	ENSP00000504984.1:n.1644-149_1644-146delinsCTCT
ENST00000681282.1:c.*1618-149_*1618-146delinsCTCT	ENSP00000506339.1:n.*1618-149_*1618-146delinsCTCT
ENST00000333213.10:c.1431-149_1431-146delinsCTCT	ENSP00000327487.6:n.1431-149_1431-146delinsCTCT
ENST00000545228.2:c.708-149_708-146delinsCTCT
ENST00000577197.1:n.179-149_179-146delinsCTCT
ENST00000579449.1:n.628-149_628-146delinsCTCT
NM_207346.2:c.1431-149_1431-146delinsCTCT	NP_997229.2:n.1431-149_1431-146delinsCTCT
XM_005257229.2:c.1619-149_1619-146delinsCTCT	XP_005257286.1:n.1619-149_1619-146delinsCTCT
XM_006721821.2:c.1316-149_1316-146delinsCTCT	XP_006721884.1:n.1316-149_1316-146delinsCTCT
XM_011524616.1:c.1502-149_1502-146delinsCTCT	XP_011522918.1:n.1502-149_1502-146delinsCTCT
XM_011524617.1:c.*13-149_*13-146delinsCTCT	XP_011522919.1:n.*13-149_*13-146delinsCTCT
XM_011524618.1:c.1314-149_1314-146delinsCTCT	XP_011522920.1:n.1314-149_1314-146delinsCTCT
XR_243646.2:n.1663-149_1663-146delinsCTCT
XM_005257229.4:c.1619-149_1619-146delinsCTCT	XP_005257286.1:n.1619-149_1619-146delinsCTCT
XR_001753015.1:n.87+195_87+198delinsAGAG
XR_001753016.1:n.88+195_88+198delinsAGAG
XR_243646.4:n.1669-149_1669-146delinsCTCT
NM_207346.3:c.1431-149_1431-146delinsCTCT MANE Select	NP_997229.2:n.1431-149_1431-146delinsCTCT