Canonical Allele Identifier: CA2275552710

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524606C= , CM000679.2:g.75524606C=	GRCh38
NC_000017.10:g.73520687C= , CM000679.1:g.73520687C=	GRCh37
NC_000017.9:g.71032282C=	NCBI36
NG_013041.1:g.13079C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*194C= MANE Select	ENSP00000327487.6:n.*194C=
ENST00000434205.8:c.*194C=	ENSP00000406559.4:n.*194C=
ENST00000545228.3:c.*274C=	ENSP00000438169.3:n.*274C=
ENST00000577197.2:n.973C=
ENST00000579449.2:n.2515C=
ENST00000580013.6:n.2919C=
ENST00000679370.1:n.3297C=
ENST00000679429.1:c.*1233C=	ENSP00000505403.1:n.*1233C=
ENST00000679443.1:n.1844C=
ENST00000679782.1:c.*474C=	ENSP00000505995.1:n.*474C=
ENST00000679919.1:n.2046C=
ENST00000679928.1:c.*2327C=	ENSP00000506071.1:n.*2327C=
ENST00000680999.1:c.*194C=	ENSP00000504984.1:n.*194C=
ENST00000681282.1:c.*1962C=	ENSP00000506339.1:n.*1962C=
ENST00000333213.10:c.*194C=	ENSP00000327487.6:n.*194C=
ENST00000545228.2:c.1052C=
ENST00000577197.1:n.523C=
NM_207346.2:c.*194C=	NP_997229.2:n.*194C=
XM_005257229.2:c.*274C=	XP_005257286.1:n.*274C=
XM_006721821.2:c.*274C=	XP_006721884.1:n.*274C=
XM_011524616.1:c.*274C=	XP_011522918.1:n.*274C=
XM_011524618.1:c.*194C=	XP_011522920.1:n.*194C=
XR_243646.2:n.2007C=
XM_005257229.4:c.*274C=	XP_005257286.1:n.*274C=
XR_243646.4:n.2013C=
NM_207346.3:c.*194C= MANE Select	NP_997229.2:n.*194C=