Canonical Allele Identifier: CA2275548463

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516784A= , CM000679.2:g.75516784A=	GRCh38
NC_000017.10:g.73512865A= , CM000679.1:g.73512865A=	GRCh37
NC_000017.9:g.71024460A=	NCBI36
NG_013041.1:g.5257A=
NG_033152.1:g.3800T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.95A= MANE Select	ENSP00000327487.6:p.Lys32=
ENST00000434205.8:c.-82-225A=	ENSP00000406559.4:n.-82-225A=
ENST00000545228.3:c.95A=	ENSP00000438169.3:p.Lys32=
ENST00000579449.2:n.20+168A=
ENST00000580013.6:n.104A=
ENST00000583818.2:c.95A=	ENSP00000461928.2:p.Lys32=
ENST00000679370.1:n.482A=
ENST00000679429.1:c.95A=	ENSP00000505403.1:p.Lys32=
ENST00000679782.1:c.95A=	ENSP00000505995.1:p.Lys32=
ENST00000679928.1:c.95A=	ENSP00000506071.1:p.Lys32=
ENST00000680528.1:n.120A=
ENST00000680999.1:c.95A=	ENSP00000504984.1:p.Lys32=
ENST00000681282.1:c.95A=	ENSP00000506339.1:p.Lys32=
ENST00000333213.10:c.95A=	ENSP00000327487.6:p.Lys32=
ENST00000434205.7:c.-82-225A=	ENSP00000406559.3:n.-82-225A=
ENST00000580013.5:n.120A=
ENST00000583173.5:c.56+168A=	ENSP00000463619.1:n.56+168A=
ENST00000583454.1:n.130A=
NM_207346.2:c.95A=	NP_997229.2:p.Lys32=
XM_005257229.2:c.95A=	XP_005257286.1:p.Lys32=
XM_006721821.2:c.-209A=	XP_006721884.1:n.-209A=
XM_011524616.1:c.95A=	XP_011522918.1:p.Lys32=
XM_011524617.1:c.95A=	XP_011522919.1:p.Lys32=
XM_011524618.1:c.95A=	XP_011522920.1:p.Lys32=
XR_243646.2:n.125A=
XM_005257229.4:c.95A=	XP_005257286.1:p.Lys32=
XR_243646.4:n.131A=
NM_207346.3:c.95A= MANE Select	NP_997229.2:p.Lys32=