Canonical Allele Identifier: CA2275552716

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524613G= , CM000679.2:g.75524613G=	GRCh38
NC_000017.10:g.73520694G= , CM000679.1:g.73520694G=	GRCh37
NC_000017.9:g.71032289G=	NCBI36
NG_013041.1:g.13086G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*201G= MANE Select	ENSP00000327487.6:n.*201G=
ENST00000434205.8:c.*201G=	ENSP00000406559.4:n.*201G=
ENST00000545228.3:c.*281G=	ENSP00000438169.3:n.*281G=
ENST00000577197.2:n.980G=
ENST00000579449.2:n.2522G=
ENST00000580013.6:n.2926G=
ENST00000679370.1:n.3304G=
ENST00000679429.1:c.*1240G=	ENSP00000505403.1:n.*1240G=
ENST00000679443.1:n.1851G=
ENST00000679782.1:c.*481G=	ENSP00000505995.1:n.*481G=
ENST00000679919.1:n.2053G=
ENST00000679928.1:c.*2334G=	ENSP00000506071.1:n.*2334G=
ENST00000680999.1:c.*201G=	ENSP00000504984.1:n.*201G=
ENST00000681282.1:c.*1969G=	ENSP00000506339.1:n.*1969G=
ENST00000333213.10:c.*201G=	ENSP00000327487.6:n.*201G=
ENST00000545228.2:c.1059G=
ENST00000577197.1:n.530G=
NM_207346.2:c.*201G=	NP_997229.2:n.*201G=
XM_005257229.2:c.*281G=	XP_005257286.1:n.*281G=
XM_006721821.2:c.*281G=	XP_006721884.1:n.*281G=
XM_011524616.1:c.*281G=	XP_011522918.1:n.*281G=
XM_011524618.1:c.*201G=	XP_011522920.1:n.*201G=
XR_243646.2:n.2014G=
XM_005257229.4:c.*281G=	XP_005257286.1:n.*281G=
XR_243646.4:n.2020G=
NM_207346.3:c.*201G= MANE Select	NP_997229.2:n.*201G=