Canonical Allele Identifier: CA2275552570

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524330T= , CM000679.2:g.75524330T=	GRCh38
NC_000017.10:g.73520411T= , CM000679.1:g.73520411T=	GRCh37
NC_000017.9:g.71032006T=	NCBI36
NG_013041.1:g.12803T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1499T= MANE Select	ENSP00000327487.6:p.Leu500=
ENST00000434205.8:c.1196T=	ENSP00000406559.4:p.Leu399=
ENST00000545228.3:c.1687T=	ENSP00000438169.3:p.Ter563=
ENST00000577197.2:n.697T=
ENST00000579449.2:n.2239T=
ENST00000580013.6:n.2643T=
ENST00000679370.1:n.3021T=
ENST00000679429.1:c.*957T=	ENSP00000505403.1:n.*957T=
ENST00000679443.1:n.1568T=
ENST00000679782.1:c.*198T=	ENSP00000505995.1:n.*198T=
ENST00000679919.1:n.1770T=
ENST00000679928.1:c.*2051T=	ENSP00000506071.1:n.*2051T=
ENST00000680528.1:n.2465T=
ENST00000680999.1:c.1712T=	ENSP00000504984.1:p.Leu571=
ENST00000681282.1:c.*1686T=	ENSP00000506339.1:n.*1686T=
ENST00000333213.10:c.1499T=	ENSP00000327487.6:p.Leu500=
ENST00000545228.2:c.776T=
ENST00000577197.1:n.247T=
ENST00000579449.1:n.696T=
NM_207346.2:c.1499T=	NP_997229.2:p.Leu500=
XM_005257229.2:c.1687T=	XP_005257286.1:p.Ter563=
XM_006721821.2:c.1384T=	XP_006721884.1:p.Ter462=
XM_011524616.1:c.1570T=	XP_011522918.1:p.Ter524=
XM_011524617.1:c.*81T=	XP_011522919.1:n.*81T=
XM_011524618.1:c.1382T=	XP_011522920.1:p.Leu461=
XR_243646.2:n.1731T=
XM_005257229.4:c.1687T=	XP_005257286.1:p.Ter563=
XR_001753015.1:n.68A=
XR_001753016.1:n.69A=
XR_243646.4:n.1737T=
NM_207346.3:c.1499T= MANE Select	NP_997229.2:p.Leu500=