Canonical Allele Identifier: CA2275552658

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524500G= , CM000679.2:g.75524500G=	GRCh38
NC_000017.10:g.73520581G= , CM000679.1:g.73520581G=	GRCh37
NC_000017.9:g.71032176G=	NCBI36
NG_013041.1:g.12973G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*88G= MANE Select	ENSP00000327487.6:n.*88G=
ENST00000434205.8:c.*88G=	ENSP00000406559.4:n.*88G=
ENST00000545228.3:c.*168G=	ENSP00000438169.3:n.*168G=
ENST00000577197.2:n.867G=
ENST00000579449.2:n.2409G=
ENST00000580013.6:n.2813G=
ENST00000679370.1:n.3191G=
ENST00000679429.1:c.*1127G=	ENSP00000505403.1:n.*1127G=
ENST00000679443.1:n.1738G=
ENST00000679782.1:c.*368G=	ENSP00000505995.1:n.*368G=
ENST00000679919.1:n.1940G=
ENST00000679928.1:c.*2221G=	ENSP00000506071.1:n.*2221G=
ENST00000680999.1:c.*88G=	ENSP00000504984.1:n.*88G=
ENST00000681282.1:c.*1856G=	ENSP00000506339.1:n.*1856G=
ENST00000333213.10:c.*88G=	ENSP00000327487.6:n.*88G=
ENST00000545228.2:c.946G=
ENST00000577197.1:n.417G=
NM_207346.2:c.*88G=	NP_997229.2:n.*88G=
XM_005257229.2:c.*168G=	XP_005257286.1:n.*168G=
XM_006721821.2:c.*168G=	XP_006721884.1:n.*168G=
XM_011524616.1:c.*168G=	XP_011522918.1:n.*168G=
XM_011524618.1:c.*88G=	XP_011522920.1:n.*88G=
XR_243646.2:n.1901G=
XM_005257229.4:c.*168G=	XP_005257286.1:n.*168G=
XR_243646.4:n.1907G=
NM_207346.3:c.*88G= MANE Select	NP_997229.2:n.*88G=