Canonical Allele Identifier: CA2275552769

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524696G= , CM000679.2:g.75524696G=	GRCh38
NC_000017.10:g.73520777G= , CM000679.1:g.73520777G=	GRCh37
NC_000017.9:g.71032372G=	NCBI36
NG_013041.1:g.13169G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*284G= MANE Select	ENSP00000327487.6:n.*284G=
ENST00000434205.8:c.*284G=	ENSP00000406559.4:n.*284G=
ENST00000577197.2:n.1063G=
ENST00000579449.2:n.2605G=
ENST00000580013.6:n.3009G=
ENST00000679370.1:n.3387G=
ENST00000679429.1:c.*1323G=	ENSP00000505403.1:n.*1323G=
ENST00000679443.1:n.1934G=
ENST00000679782.1:c.*564G=	ENSP00000505995.1:n.*564G=
ENST00000679919.1:n.2136G=
ENST00000679928.1:c.*2417G=	ENSP00000506071.1:n.*2417G=
ENST00000680999.1:c.*284G=	ENSP00000504984.1:n.*284G=
ENST00000681282.1:c.*2052G=	ENSP00000506339.1:n.*2052G=
ENST00000333213.10:c.*284G=	ENSP00000327487.6:n.*284G=
ENST00000577197.1:n.613G=
NM_207346.2:c.*284G=	NP_997229.2:n.*284G=
XM_005257229.2:c.*364G=	XP_005257286.1:n.*364G=
XM_006721821.2:c.*364G=	XP_006721884.1:n.*364G=
XM_011524616.1:c.*364G=	XP_011522918.1:n.*364G=
XM_011524618.1:c.*284G=	XP_011522920.1:n.*284G=
XR_243646.2:n.2097G=
XM_005257229.4:c.*364G=	XP_005257286.1:n.*364G=
XR_243646.4:n.2103G=
NM_207346.3:c.*284G= MANE Select	NP_997229.2:n.*284G=