Canonical Allele Identifier: CA2275552635

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524467C= , CM000679.2:g.75524467C=	GRCh38
NC_000017.10:g.73520548C= , CM000679.1:g.73520548C=	GRCh37
NC_000017.9:g.71032143C=	NCBI36
NG_013041.1:g.12940C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*55C= MANE Select	ENSP00000327487.6:n.*55C=
ENST00000434205.8:c.*55C=	ENSP00000406559.4:n.*55C=
ENST00000545228.3:c.*135C=	ENSP00000438169.3:n.*135C=
ENST00000577197.2:n.834C=
ENST00000579449.2:n.2376C=
ENST00000580013.6:n.2780C=
ENST00000679370.1:n.3158C=
ENST00000679429.1:c.*1094C=	ENSP00000505403.1:n.*1094C=
ENST00000679443.1:n.1705C=
ENST00000679782.1:c.*335C=	ENSP00000505995.1:n.*335C=
ENST00000679919.1:n.1907C=
ENST00000679928.1:c.*2188C=	ENSP00000506071.1:n.*2188C=
ENST00000680999.1:c.*55C=	ENSP00000504984.1:n.*55C=
ENST00000681282.1:c.*1823C=	ENSP00000506339.1:n.*1823C=
ENST00000333213.10:c.*55C=	ENSP00000327487.6:n.*55C=
ENST00000545228.2:c.913C=
ENST00000577197.1:n.384C=
NM_207346.2:c.*55C=	NP_997229.2:n.*55C=
XM_005257229.2:c.*135C=	XP_005257286.1:n.*135C=
XM_006721821.2:c.*135C=	XP_006721884.1:n.*135C=
XM_011524616.1:c.*135C=	XP_011522918.1:n.*135C=
XM_011524618.1:c.*55C=	XP_011522920.1:n.*55C=
XR_243646.2:n.1868C=
XM_005257229.4:c.*135C=	XP_005257286.1:n.*135C=
XR_243646.4:n.1874C=
NM_207346.3:c.*55C= MANE Select	NP_997229.2:n.*55C=