Canonical Allele Identifier: CA2275552771

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524702T= , CM000679.2:g.75524702T=	GRCh38
NC_000017.10:g.73520783T= , CM000679.1:g.73520783T=	GRCh37
NC_000017.9:g.71032378T=	NCBI36
NG_013041.1:g.13175T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*290T= MANE Select	ENSP00000327487.6:n.*290T=
ENST00000434205.8:c.*290T=	ENSP00000406559.4:n.*290T=
ENST00000577197.2:n.1069T=
ENST00000579449.2:n.2611T=
ENST00000580013.6:n.3015T=
ENST00000679370.1:n.3393T=
ENST00000679429.1:c.*1329T=	ENSP00000505403.1:n.*1329T=
ENST00000679928.1:c.*2423T=	ENSP00000506071.1:n.*2423T=
ENST00000681282.1:c.*2058T=	ENSP00000506339.1:n.*2058T=
ENST00000333213.10:c.*290T=	ENSP00000327487.6:n.*290T=
ENST00000577197.1:n.619T=
NM_207346.2:c.*290T=	NP_997229.2:n.*290T=
XM_005257229.2:c.*370T=	XP_005257286.1:n.*370T=
XM_006721821.2:c.*370T=	XP_006721884.1:n.*370T=
XM_011524616.1:c.*370T=	XP_011522918.1:n.*370T=
XM_011524618.1:c.*290T=	XP_011522920.1:n.*290T=
XR_243646.2:n.2103T=
XM_005257229.4:c.*370T=	XP_005257286.1:n.*370T=
XR_243646.4:n.2109T=
NM_207346.3:c.*290T= MANE Select	NP_997229.2:n.*290T=