Canonical Allele Identifier: CA2275551252

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521844G= , CM000679.2:g.75521844G=	GRCh38
NC_000017.10:g.73517925G= , CM000679.1:g.73517925G=	GRCh37
NC_000017.9:g.71029520G=	NCBI36
NG_013041.1:g.10317G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.763G= MANE Select	ENSP00000327487.6:p.Gly255=
ENST00000434205.8:c.460G=	ENSP00000406559.4:p.Gly154=
ENST00000545228.3:c.763G=	ENSP00000438169.3:p.Gly255=
ENST00000579449.2:n.562G=
ENST00000580013.6:n.966G=
ENST00000583818.2:c.817G=	ENSP00000461928.2:n.817G=
ENST00000679370.1:n.1344G=
ENST00000679429.1:c.*221G=	ENSP00000505403.1:n.*221G=
ENST00000679443.1:n.832G=
ENST00000679782.1:c.763G=	ENSP00000505995.1:p.Gly255=
ENST00000679919.1:n.832G=
ENST00000679928.1:c.*374G=	ENSP00000506071.1:n.*374G=
ENST00000680528.1:n.788G=
ENST00000680999.1:c.763G=	ENSP00000504984.1:p.Gly255=
ENST00000681282.1:c.*9G=	ENSP00000506339.1:n.*9G=
ENST00000333213.10:c.763G=	ENSP00000327487.6:p.Gly255=
ENST00000578415.1:c.723G=
ENST00000583173.5:c.459-163G=	ENSP00000463619.1:n.459-163G=
ENST00000583818.1:c.712G=	ENSP00000461928.1:n.712G=
NM_207346.2:c.763G=	NP_997229.2:p.Gly255=
XM_005257229.2:c.763G=	XP_005257286.1:p.Gly255=
XM_006721821.2:c.460G=	XP_006721884.1:p.Gly154=
XM_011524616.1:c.763G=	XP_011522918.1:p.Gly255=
XM_011524617.1:c.763G=	XP_011522919.1:p.Gly255=
XM_011524618.1:c.763G=	XP_011522920.1:p.Gly255=
XR_243646.2:n.793G=
XM_005257229.4:c.763G=	XP_005257286.1:p.Gly255=
XR_243646.4:n.799G=
NM_207346.3:c.763G= MANE Select	NP_997229.2:p.Gly255=