Canonical Allele Identifier: CA2275552572

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524332A= , CM000679.2:g.75524332A=	GRCh38
NC_000017.10:g.73520413A= , CM000679.1:g.73520413A=	GRCh37
NC_000017.9:g.71032008A=	NCBI36
NG_013041.1:g.12805A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1501A= MANE Select	ENSP00000327487.6:p.Ile501=
ENST00000434205.8:c.1198A=	ENSP00000406559.4:p.Ile400=
ENST00000545228.3:c.1689A=	ENSP00000438169.3:p.Ter563=
ENST00000577197.2:n.699A=
ENST00000579449.2:n.2241A=
ENST00000580013.6:n.2645A=
ENST00000679370.1:n.3023A=
ENST00000679429.1:c.*959A=	ENSP00000505403.1:n.*959A=
ENST00000679443.1:n.1570A=
ENST00000679782.1:c.*200A=	ENSP00000505995.1:n.*200A=
ENST00000679919.1:n.1772A=
ENST00000679928.1:c.*2053A=	ENSP00000506071.1:n.*2053A=
ENST00000680528.1:n.2467A=
ENST00000680999.1:c.1714A=	ENSP00000504984.1:p.Ile572=
ENST00000681282.1:c.*1688A=	ENSP00000506339.1:n.*1688A=
ENST00000333213.10:c.1501A=	ENSP00000327487.6:p.Ile501=
ENST00000545228.2:c.778A=
ENST00000577197.1:n.249A=
ENST00000579449.1:n.698A=
NM_207346.2:c.1501A=	NP_997229.2:p.Ile501=
XM_005257229.2:c.1689A=	XP_005257286.1:p.Ter563=
XM_006721821.2:c.1386A=	XP_006721884.1:p.Ter462=
XM_011524616.1:c.1572A=	XP_011522918.1:p.Ter524=
XM_011524617.1:c.*83A=	XP_011522919.1:n.*83A=
XM_011524618.1:c.1384A=	XP_011522920.1:p.Ile462=
XR_243646.2:n.1733A=
XM_005257229.4:c.1689A=	XP_005257286.1:p.Ter563=
XR_001753015.1:n.66T=
XR_001753016.1:n.67T=
XR_243646.4:n.1739A=
NM_207346.3:c.1501A= MANE Select	NP_997229.2:p.Ile501=