Canonical Allele Identifier: CA2275552609

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524408A= , CM000679.2:g.75524408A=	GRCh38
NC_000017.10:g.73520489A= , CM000679.1:g.73520489A=	GRCh37
NC_000017.9:g.71032084A=	NCBI36
NG_013041.1:g.12881A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1577A= MANE Select	ENSP00000327487.6:p.His526=
ENST00000434205.8:c.1274A=	ENSP00000406559.4:p.His425=
ENST00000545228.3:c.*76A=	ENSP00000438169.3:n.*76A=
ENST00000577197.2:n.775A=
ENST00000579449.2:n.2317A=
ENST00000580013.6:n.2721A=
ENST00000679370.1:n.3099A=
ENST00000679429.1:c.*1035A=	ENSP00000505403.1:n.*1035A=
ENST00000679443.1:n.1646A=
ENST00000679782.1:c.*276A=	ENSP00000505995.1:n.*276A=
ENST00000679919.1:n.1848A=
ENST00000679928.1:c.*2129A=	ENSP00000506071.1:n.*2129A=
ENST00000680528.1:n.2543A=
ENST00000680999.1:c.1790A=	ENSP00000504984.1:p.His597=
ENST00000681282.1:c.*1764A=	ENSP00000506339.1:n.*1764A=
ENST00000333213.10:c.1577A=	ENSP00000327487.6:p.His526=
ENST00000545228.2:c.854A=
ENST00000577197.1:n.325A=
ENST00000579449.1:n.774A=
NM_207346.2:c.1577A=	NP_997229.2:p.His526=
XM_005257229.2:c.*76A=	XP_005257286.1:n.*76A=
XM_006721821.2:c.*76A=	XP_006721884.1:n.*76A=
XM_011524616.1:c.*76A=	XP_011522918.1:n.*76A=
XM_011524618.1:c.1460A=	XP_011522920.1:p.His487=
XR_243646.2:n.1809A=
XM_005257229.4:c.*76A=	XP_005257286.1:n.*76A=
XR_243646.4:n.1815A=
NM_207346.3:c.1577A= MANE Select	NP_997229.2:p.His526=