Canonical Allele Identifier: CA2275552706

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524592C= , CM000679.2:g.75524592C=	GRCh38
NC_000017.10:g.73520673C= , CM000679.1:g.73520673C=	GRCh37
NC_000017.9:g.71032268C=	NCBI36
NG_013041.1:g.13065C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*180C= MANE Select	ENSP00000327487.6:n.*180C=
ENST00000434205.8:c.*180C=	ENSP00000406559.4:n.*180C=
ENST00000545228.3:c.*260C=	ENSP00000438169.3:n.*260C=
ENST00000577197.2:n.959C=
ENST00000579449.2:n.2501C=
ENST00000580013.6:n.2905C=
ENST00000679370.1:n.3283C=
ENST00000679429.1:c.*1219C=	ENSP00000505403.1:n.*1219C=
ENST00000679443.1:n.1830C=
ENST00000679782.1:c.*460C=	ENSP00000505995.1:n.*460C=
ENST00000679919.1:n.2032C=
ENST00000679928.1:c.*2313C=	ENSP00000506071.1:n.*2313C=
ENST00000680999.1:c.*180C=	ENSP00000504984.1:n.*180C=
ENST00000681282.1:c.*1948C=	ENSP00000506339.1:n.*1948C=
ENST00000333213.10:c.*180C=	ENSP00000327487.6:n.*180C=
ENST00000545228.2:c.1038C=
ENST00000577197.1:n.509C=
NM_207346.2:c.*180C=	NP_997229.2:n.*180C=
XM_005257229.2:c.*260C=	XP_005257286.1:n.*260C=
XM_006721821.2:c.*260C=	XP_006721884.1:n.*260C=
XM_011524616.1:c.*260C=	XP_011522918.1:n.*260C=
XM_011524618.1:c.*180C=	XP_011522920.1:n.*180C=
XR_243646.2:n.1993C=
XM_005257229.4:c.*260C=	XP_005257286.1:n.*260C=
XR_243646.4:n.1999C=
NM_207346.3:c.*180C= MANE Select	NP_997229.2:n.*180C=