Canonical Allele Identifier: CA2275552682

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524559A= , CM000679.2:g.75524559A=	GRCh38
NC_000017.10:g.73520640A= , CM000679.1:g.73520640A=	GRCh37
NC_000017.9:g.71032235A=	NCBI36
NG_013041.1:g.13032A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*147A= MANE Select	ENSP00000327487.6:n.*147A=
ENST00000434205.8:c.*147A=	ENSP00000406559.4:n.*147A=
ENST00000545228.3:c.*227A=	ENSP00000438169.3:n.*227A=
ENST00000577197.2:n.926A=
ENST00000579449.2:n.2468A=
ENST00000580013.6:n.2872A=
ENST00000679370.1:n.3250A=
ENST00000679429.1:c.*1186A=	ENSP00000505403.1:n.*1186A=
ENST00000679443.1:n.1797A=
ENST00000679782.1:c.*427A=	ENSP00000505995.1:n.*427A=
ENST00000679919.1:n.1999A=
ENST00000679928.1:c.*2280A=	ENSP00000506071.1:n.*2280A=
ENST00000680999.1:c.*147A=	ENSP00000504984.1:n.*147A=
ENST00000681282.1:c.*1915A=	ENSP00000506339.1:n.*1915A=
ENST00000333213.10:c.*147A=	ENSP00000327487.6:n.*147A=
ENST00000545228.2:c.1005A=
ENST00000577197.1:n.476A=
NM_207346.2:c.*147A=	NP_997229.2:n.*147A=
XM_005257229.2:c.*227A=	XP_005257286.1:n.*227A=
XM_006721821.2:c.*227A=	XP_006721884.1:n.*227A=
XM_011524616.1:c.*227A=	XP_011522918.1:n.*227A=
XM_011524618.1:c.*147A=	XP_011522920.1:n.*147A=
XR_243646.2:n.1960A=
XM_005257229.4:c.*227A=	XP_005257286.1:n.*227A=
XR_243646.4:n.1966A=
NM_207346.3:c.*147A= MANE Select	NP_997229.2:n.*147A=