Canonical Allele Identifier: CA2275552421

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524005A= , CM000679.2:g.75524005A=	GRCh38
NC_000017.10:g.73520086A= , CM000679.1:g.73520086A=	GRCh37
NC_000017.9:g.71031681A=	NCBI36
NG_013041.1:g.12478A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1430+226A= MANE Select	ENSP00000327487.6:n.1430+226A=
ENST00000434205.8:c.1127+226A=	ENSP00000406559.4:n.1127+226A=
ENST00000545228.3:c.1618+226A=	ENSP00000438169.3:n.1618+226A=
ENST00000577197.2:n.628+226A=
ENST00000579449.2:n.2170+226A=
ENST00000580013.6:n.2574+226A=
ENST00000679370.1:n.2952+226A=
ENST00000679429.1:c.*888+226A=	ENSP00000505403.1:n.*888+226A=
ENST00000679443.1:n.1499+226A=
ENST00000679782.1:c.*129+226A=	ENSP00000505995.1:n.*129+226A=
ENST00000679919.1:n.1701+226A=
ENST00000679928.1:c.*1982+226A=	ENSP00000506071.1:n.*1982+226A=
ENST00000680528.1:n.2396+226A=
ENST00000680999.1:c.1643+226A=	ENSP00000504984.1:n.1643+226A=
ENST00000681282.1:c.*1617+226A=	ENSP00000506339.1:n.*1617+226A=
ENST00000333213.10:c.1430+226A=	ENSP00000327487.6:n.1430+226A=
ENST00000545228.2:c.707+226A=
ENST00000577197.1:n.178+226A=
ENST00000579449.1:n.627+226A=
NM_207346.2:c.1430+226A=	NP_997229.2:n.1430+226A=
XM_005257229.2:c.1618+226A=	XP_005257286.1:n.1618+226A=
XM_006721821.2:c.1315+226A=	XP_006721884.1:n.1315+226A=
XM_011524616.1:c.1502-257A=	XP_011522918.1:n.1502-257A=
XM_011524617.1:c.*13-257A=	XP_011522919.1:n.*13-257A=
XM_011524618.1:c.1314-257A=	XP_011522920.1:n.1314-257A=
XR_243646.2:n.1662+226A=
XM_005257229.4:c.1618+226A=	XP_005257286.1:n.1618+226A=
XR_001753015.1:n.87+306T=
XR_001753016.1:n.88+306T=
XR_243646.4:n.1668+226A=
NM_207346.3:c.1430+226A= MANE Select	NP_997229.2:n.1430+226A=