Canonical Allele Identifier: CA2839025332

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75522195dup , CM000679.2:g.75522195dup	GRCh38
NC_000017.10:g.73518276dup , CM000679.1:g.73518276dup	GRCh37
NC_000017.9:g.71029871dup	NCBI36
NG_013041.1:g.10668dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1114dup MANE Select	ENSP00000327487.6:p.Val372GlyfsTer?
ENST00000434205.8:c.811dup	ENSP00000406559.4:p.Val271GlyfsTer?
ENST00000545228.3:c.1114dup	ENSP00000438169.3:p.Val372GlyfsTer?
ENST00000579449.2:n.913dup
ENST00000580013.6:n.1317dup
ENST00000679370.1:n.1695dup
ENST00000679429.1:c.*572dup	ENSP00000505403.1:n.*572dup
ENST00000679443.1:n.1183dup
ENST00000679782.1:c.1114dup	ENSP00000505995.1:p.Val372GlyfsTer?
ENST00000679919.1:n.1183dup
ENST00000679928.1:c.*725dup	ENSP00000506071.1:n.*725dup
ENST00000680528.1:n.1139dup
ENST00000680999.1:c.1114dup	ENSP00000504984.1:p.Val372GlyfsTer?
ENST00000681282.1:c.*360dup	ENSP00000506339.1:n.*360dup
ENST00000333213.10:c.1114dup	ENSP00000327487.6:p.Val372GlyfsTer?
ENST00000545228.2:c.203dup
ENST00000583173.5:c.647dup	ENSP00000463619.1:n.647dup
NM_207346.2:c.1114dup	NP_997229.2:p.Val372GlyfsTer?
XM_005257229.2:c.1114dup	XP_005257286.1:p.Val372GlyfsTer?
XM_006721821.2:c.811dup	XP_006721884.1:p.Val271GlyfsTer?
XM_011524616.1:c.1114dup	XP_011522918.1:p.Val372GlyfsTer?
XM_011524617.1:c.1114dup	XP_011522919.1:p.Val372GlyfsTer?
XM_011524618.1:c.1114dup	XP_011522920.1:p.Val372GlyfsTer?
XR_243646.2:n.1144dup
XM_005257229.4:c.1114dup	XP_005257286.1:p.Val372GlyfsTer?
XR_243646.4:n.1150dup
NM_207346.3:c.1114dup MANE Select	NP_997229.2:p.Val372GlyfsTer?