Canonical Allele Identifier: CA2275552758

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524684G= , CM000679.2:g.75524684G=	GRCh38
NC_000017.10:g.73520765G= , CM000679.1:g.73520765G=	GRCh37
NC_000017.9:g.71032360G=	NCBI36
NG_013041.1:g.13157G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*272G= MANE Select	ENSP00000327487.6:n.*272G=
ENST00000434205.8:c.*272G=	ENSP00000406559.4:n.*272G=
ENST00000545228.3:c.*352G=	ENSP00000438169.3:n.*352G=
ENST00000577197.2:n.1051G=
ENST00000579449.2:n.2593G=
ENST00000580013.6:n.2997G=
ENST00000679370.1:n.3375G=
ENST00000679429.1:c.*1311G=	ENSP00000505403.1:n.*1311G=
ENST00000679443.1:n.1922G=
ENST00000679782.1:c.*552G=	ENSP00000505995.1:n.*552G=
ENST00000679919.1:n.2124G=
ENST00000679928.1:c.*2405G=	ENSP00000506071.1:n.*2405G=
ENST00000680999.1:c.*272G=	ENSP00000504984.1:n.*272G=
ENST00000681282.1:c.*2040G=	ENSP00000506339.1:n.*2040G=
ENST00000333213.10:c.*272G=	ENSP00000327487.6:n.*272G=
ENST00000545228.2:c.1130G=
ENST00000577197.1:n.601G=
NM_207346.2:c.*272G=	NP_997229.2:n.*272G=
XM_005257229.2:c.*352G=	XP_005257286.1:n.*352G=
XM_006721821.2:c.*352G=	XP_006721884.1:n.*352G=
XM_011524616.1:c.*352G=	XP_011522918.1:n.*352G=
XM_011524618.1:c.*272G=	XP_011522920.1:n.*272G=
XR_243646.2:n.2085G=
XM_005257229.4:c.*352G=	XP_005257286.1:n.*352G=
XR_243646.4:n.2091G=
NM_207346.3:c.*272G= MANE Select	NP_997229.2:n.*272G=