Canonical Allele Identifier: CA2275552767

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524695C= , CM000679.2:g.75524695C=	GRCh38
NC_000017.10:g.73520776C= , CM000679.1:g.73520776C=	GRCh37
NC_000017.9:g.71032371C=	NCBI36
NG_013041.1:g.13168C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*283C= MANE Select	ENSP00000327487.6:n.*283C=
ENST00000434205.8:c.*283C=	ENSP00000406559.4:n.*283C=
ENST00000577197.2:n.1062C=
ENST00000579449.2:n.2604C=
ENST00000580013.6:n.3008C=
ENST00000679370.1:n.3386C=
ENST00000679429.1:c.*1322C=	ENSP00000505403.1:n.*1322C=
ENST00000679443.1:n.1933C=
ENST00000679782.1:c.*563C=	ENSP00000505995.1:n.*563C=
ENST00000679919.1:n.2135C=
ENST00000679928.1:c.*2416C=	ENSP00000506071.1:n.*2416C=
ENST00000680999.1:c.*283C=	ENSP00000504984.1:n.*283C=
ENST00000681282.1:c.*2051C=	ENSP00000506339.1:n.*2051C=
ENST00000333213.10:c.*283C=	ENSP00000327487.6:n.*283C=
ENST00000577197.1:n.612C=
NM_207346.2:c.*283C=	NP_997229.2:n.*283C=
XM_005257229.2:c.*363C=	XP_005257286.1:n.*363C=
XM_006721821.2:c.*363C=	XP_006721884.1:n.*363C=
XM_011524616.1:c.*363C=	XP_011522918.1:n.*363C=
XM_011524618.1:c.*283C=	XP_011522920.1:n.*283C=
XR_243646.2:n.2096C=
XM_005257229.4:c.*363C=	XP_005257286.1:n.*363C=
XR_243646.4:n.2102C=
NM_207346.3:c.*283C= MANE Select	NP_997229.2:n.*283C=