Canonical Allele Identifier: CA2275552559

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524312A= , CM000679.2:g.75524312A=	GRCh38
NC_000017.10:g.73520393A= , CM000679.1:g.73520393A=	GRCh37
NC_000017.9:g.71031988A=	NCBI36
NG_013041.1:g.12785A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1481A= MANE Select	ENSP00000327487.6:p.Gln494=
ENST00000434205.8:c.1178A=	ENSP00000406559.4:p.Gln393=
ENST00000545228.3:c.1669A=	ENSP00000438169.3:p.Arg557=
ENST00000577197.2:n.679A=
ENST00000579449.2:n.2221A=
ENST00000580013.6:n.2625A=
ENST00000679370.1:n.3003A=
ENST00000679429.1:c.*939A=	ENSP00000505403.1:n.*939A=
ENST00000679443.1:n.1550A=
ENST00000679782.1:c.*180A=	ENSP00000505995.1:n.*180A=
ENST00000679919.1:n.1752A=
ENST00000679928.1:c.*2033A=	ENSP00000506071.1:n.*2033A=
ENST00000680528.1:n.2447A=
ENST00000680999.1:c.1694A=	ENSP00000504984.1:p.Gln565=
ENST00000681282.1:c.*1668A=	ENSP00000506339.1:n.*1668A=
ENST00000333213.10:c.1481A=	ENSP00000327487.6:p.Gln494=
ENST00000545228.2:c.758A=
ENST00000577197.1:n.229A=
ENST00000579449.1:n.678A=
NM_207346.2:c.1481A=	NP_997229.2:p.Gln494=
XM_005257229.2:c.1669A=	XP_005257286.1:p.Arg557=
XM_006721821.2:c.1366A=	XP_006721884.1:p.Arg456=
XM_011524616.1:c.1552A=	XP_011522918.1:p.Arg518=
XM_011524617.1:c.*63A=	XP_011522919.1:n.*63A=
XM_011524618.1:c.1364A=	XP_011522920.1:p.Gln455=
XR_243646.2:n.1713A=
XM_005257229.4:c.1669A=	XP_005257286.1:p.Arg557=
XR_001753015.1:n.86T=
XR_001753016.1:n.87T=
XR_243646.4:n.1719A=
NM_207346.3:c.1481A= MANE Select	NP_997229.2:p.Gln494=