Canonical Allele Identifier: CA2275551202

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521753G= , CM000679.2:g.75521753G=	GRCh38
NC_000017.10:g.73517834G= , CM000679.1:g.73517834G=	GRCh37
NC_000017.9:g.71029429G=	NCBI36
NG_013041.1:g.10226G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.672G= MANE Select	ENSP00000327487.6:p.Lys224=
ENST00000434205.8:c.369G=	ENSP00000406559.4:p.Lys123=
ENST00000545228.3:c.672G=	ENSP00000438169.3:p.Lys224=
ENST00000579449.2:n.471G=
ENST00000580013.6:n.875G=
ENST00000583818.2:c.726G=	ENSP00000461928.2:n.726G=
ENST00000679370.1:n.1253G=
ENST00000679429.1:c.*130G=	ENSP00000505403.1:n.*130G=
ENST00000679443.1:n.741G=
ENST00000679782.1:c.672G=	ENSP00000505995.1:p.Lys224=
ENST00000679919.1:n.741G=
ENST00000679928.1:c.*283G=	ENSP00000506071.1:n.*283G=
ENST00000680528.1:n.697G=
ENST00000680999.1:c.672G=	ENSP00000504984.1:p.Lys224=
ENST00000681282.1:c.701G=	ENSP00000506339.1:p.Arg234=
ENST00000333213.10:c.672G=	ENSP00000327487.6:p.Lys224=
ENST00000578415.1:c.632G=
ENST00000583173.5:c.458+243G=	ENSP00000463619.1:n.458+243G=
ENST00000583818.1:c.621G=	ENSP00000461928.1:n.621G=
NM_207346.2:c.672G=	NP_997229.2:p.Lys224=
XM_005257229.2:c.672G=	XP_005257286.1:p.Lys224=
XM_006721821.2:c.369G=	XP_006721884.1:p.Lys123=
XM_011524616.1:c.672G=	XP_011522918.1:p.Lys224=
XM_011524617.1:c.672G=	XP_011522919.1:p.Lys224=
XM_011524618.1:c.672G=	XP_011522920.1:p.Lys224=
XR_243646.2:n.702G=
XM_005257229.4:c.672G=	XP_005257286.1:p.Lys224=
XR_243646.4:n.708G=
NM_207346.3:c.672G= MANE Select	NP_997229.2:p.Lys224=