Canonical Allele Identifier: CA2275552552

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524298G= , CM000679.2:g.75524298G=	GRCh38
NC_000017.10:g.73520379G= , CM000679.1:g.73520379G=	GRCh37
NC_000017.9:g.71031974G=	NCBI36
NG_013041.1:g.12771G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1467G= MANE Select	ENSP00000327487.6:p.Lys489=
ENST00000434205.8:c.1164G=	ENSP00000406559.4:p.Lys388=
ENST00000545228.3:c.1655G=	ENSP00000438169.3:p.Ser552=
ENST00000577197.2:n.665G=
ENST00000579449.2:n.2207G=
ENST00000580013.6:n.2611G=
ENST00000679370.1:n.2989G=
ENST00000679429.1:c.*925G=	ENSP00000505403.1:n.*925G=
ENST00000679443.1:n.1536G=
ENST00000679782.1:c.*166G=	ENSP00000505995.1:n.*166G=
ENST00000679919.1:n.1738G=
ENST00000679928.1:c.*2019G=	ENSP00000506071.1:n.*2019G=
ENST00000680528.1:n.2433G=
ENST00000680999.1:c.1680G=	ENSP00000504984.1:p.Lys560=
ENST00000681282.1:c.*1654G=	ENSP00000506339.1:n.*1654G=
ENST00000333213.10:c.1467G=	ENSP00000327487.6:p.Lys489=
ENST00000545228.2:c.744G=
ENST00000577197.1:n.215G=
ENST00000579449.1:n.664G=
NM_207346.2:c.1467G=	NP_997229.2:p.Lys489=
XM_005257229.2:c.1655G=	XP_005257286.1:p.Ser552=
XM_006721821.2:c.1352G=	XP_006721884.1:p.Ser451=
XM_011524616.1:c.1538G=	XP_011522918.1:p.Ser513=
XM_011524617.1:c.*49G=	XP_011522919.1:n.*49G=
XM_011524618.1:c.1350G=	XP_011522920.1:p.Lys450=
XR_243646.2:n.1699G=
XM_005257229.4:c.1655G=	XP_005257286.1:p.Ser552=
XR_001753015.1:n.87+13C=
XR_001753016.1:n.88+13C=
XR_243646.4:n.1705G=
NM_207346.3:c.1467G= MANE Select	NP_997229.2:p.Lys489=