Canonical Allele Identifier: CA2275552389

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75523930C= , CM000679.2:g.75523930C=	GRCh38
NC_000017.10:g.73520011C= , CM000679.1:g.73520011C=	GRCh37
NC_000017.9:g.71031606C=	NCBI36
NG_013041.1:g.12403C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1430+151C= MANE Select	ENSP00000327487.6:n.1430+151C=
ENST00000434205.8:c.1127+151C=	ENSP00000406559.4:n.1127+151C=
ENST00000545228.3:c.1618+151C=	ENSP00000438169.3:n.1618+151C=
ENST00000577197.2:n.628+151C=
ENST00000579449.2:n.2170+151C=
ENST00000580013.6:n.2574+151C=
ENST00000679370.1:n.2952+151C=
ENST00000679429.1:c.*888+151C=	ENSP00000505403.1:n.*888+151C=
ENST00000679443.1:n.1499+151C=
ENST00000679782.1:c.*129+151C=	ENSP00000505995.1:n.*129+151C=
ENST00000679919.1:n.1701+151C=
ENST00000679928.1:c.*1982+151C=	ENSP00000506071.1:n.*1982+151C=
ENST00000680528.1:n.2396+151C=
ENST00000680999.1:c.1643+151C=	ENSP00000504984.1:n.1643+151C=
ENST00000681282.1:c.*1617+151C=	ENSP00000506339.1:n.*1617+151C=
ENST00000333213.10:c.1430+151C=	ENSP00000327487.6:n.1430+151C=
ENST00000545228.2:c.707+151C=
ENST00000577197.1:n.178+151C=
ENST00000579449.1:n.627+151C=
NM_207346.2:c.1430+151C=	NP_997229.2:n.1430+151C=
XM_005257229.2:c.1618+151C=	XP_005257286.1:n.1618+151C=
XM_006721821.2:c.1315+151C=	XP_006721884.1:n.1315+151C=
XM_011524616.1:c.1502-332C=	XP_011522918.1:n.1502-332C=
XM_011524617.1:c.*13-332C=	XP_011522919.1:n.*13-332C=
XM_011524618.1:c.1314-332C=	XP_011522920.1:n.1314-332C=
XR_243646.2:n.1662+151C=
XM_005257229.4:c.1618+151C=	XP_005257286.1:n.1618+151C=
XR_001753015.1:n.87+381G=
XR_001753016.1:n.88+381G=
XR_243646.4:n.1668+151C=
NM_207346.3:c.1430+151C= MANE Select	NP_997229.2:n.1430+151C=