Canonical Allele Identifier: CA2275551415

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75522094G= , CM000679.2:g.75522094G=	GRCh38
NC_000017.10:g.73518175G= , CM000679.1:g.73518175G=	GRCh37
NC_000017.9:g.71029770G=	NCBI36
NG_013041.1:g.10567G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1013G= MANE Select	ENSP00000327487.6:p.Cys338=
ENST00000434205.8:c.710G=	ENSP00000406559.4:p.Cys237=
ENST00000545228.3:c.1013G=	ENSP00000438169.3:p.Cys338=
ENST00000579449.2:n.812G=
ENST00000580013.6:n.1216G=
ENST00000679370.1:n.1594G=
ENST00000679429.1:c.*471G=	ENSP00000505403.1:n.*471G=
ENST00000679443.1:n.1082G=
ENST00000679782.1:c.1013G=	ENSP00000505995.1:p.Cys338=
ENST00000679919.1:n.1082G=
ENST00000679928.1:c.*624G=	ENSP00000506071.1:n.*624G=
ENST00000680528.1:n.1038G=
ENST00000680999.1:c.1013G=	ENSP00000504984.1:p.Cys338=
ENST00000681282.1:c.*259G=	ENSP00000506339.1:n.*259G=
ENST00000333213.10:c.1013G=	ENSP00000327487.6:p.Cys338=
ENST00000545228.2:c.102G=
ENST00000578415.1:c.973G=
ENST00000583173.5:c.546G=	ENSP00000463619.1:n.546G=
NM_207346.2:c.1013G=	NP_997229.2:p.Cys338=
XM_005257229.2:c.1013G=	XP_005257286.1:p.Cys338=
XM_006721821.2:c.710G=	XP_006721884.1:p.Cys237=
XM_011524616.1:c.1013G=	XP_011522918.1:p.Cys338=
XM_011524617.1:c.1013G=	XP_011522919.1:p.Cys338=
XM_011524618.1:c.1013G=	XP_011522920.1:p.Cys338=
XR_243646.2:n.1043G=
XM_005257229.4:c.1013G=	XP_005257286.1:p.Cys338=
XR_243646.4:n.1049G=
NM_207346.3:c.1013G= MANE Select	NP_997229.2:p.Cys338=