Canonical Allele Identifier: CA2275552634

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524462C= , CM000679.2:g.75524462C=	GRCh38
NC_000017.10:g.73520543C= , CM000679.1:g.73520543C=	GRCh37
NC_000017.9:g.71032138C=	NCBI36
NG_013041.1:g.12935C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*50C= MANE Select	ENSP00000327487.6:n.*50C=
ENST00000434205.8:c.*50C=	ENSP00000406559.4:n.*50C=
ENST00000545228.3:c.*130C=	ENSP00000438169.3:n.*130C=
ENST00000577197.2:n.829C=
ENST00000579449.2:n.2371C=
ENST00000580013.6:n.2775C=
ENST00000679370.1:n.3153C=
ENST00000679429.1:c.*1089C=	ENSP00000505403.1:n.*1089C=
ENST00000679443.1:n.1700C=
ENST00000679782.1:c.*330C=	ENSP00000505995.1:n.*330C=
ENST00000679919.1:n.1902C=
ENST00000679928.1:c.*2183C=	ENSP00000506071.1:n.*2183C=
ENST00000680999.1:c.*50C=	ENSP00000504984.1:n.*50C=
ENST00000681282.1:c.*1818C=	ENSP00000506339.1:n.*1818C=
ENST00000333213.10:c.*50C=	ENSP00000327487.6:n.*50C=
ENST00000545228.2:c.908C=
ENST00000577197.1:n.379C=
NM_207346.2:c.*50C=	NP_997229.2:n.*50C=
XM_005257229.2:c.*130C=	XP_005257286.1:n.*130C=
XM_006721821.2:c.*130C=	XP_006721884.1:n.*130C=
XM_011524616.1:c.*130C=	XP_011522918.1:n.*130C=
XM_011524618.1:c.*50C=	XP_011522920.1:n.*50C=
XR_243646.2:n.1863C=
XM_005257229.4:c.*130C=	XP_005257286.1:n.*130C=
XR_243646.4:n.1869C=
NM_207346.3:c.*50C= MANE Select	NP_997229.2:n.*50C=