Canonical Allele Identifier: CA2275551247

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521833T= , CM000679.2:g.75521833T=	GRCh38
NC_000017.10:g.73517914T= , CM000679.1:g.73517914T=	GRCh37
NC_000017.9:g.71029509T=	NCBI36
NG_013041.1:g.10306T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000333213.11:c.752T= MANE Select	ENSP00000327487.6:p.Met251=
ENST00000434205.8:c.449T=	ENSP00000406559.4:p.Met150=
ENST00000545228.3:c.752T=	ENSP00000438169.3:p.Met251=
ENST00000579449.2:n.551T=
ENST00000580013.6:n.955T=
ENST00000583818.2:c.806T=	ENSP00000461928.2:n.806T=
ENST00000679370.1:n.1333T=
ENST00000679429.1:c.*210T=	ENSP00000505403.1:n.*210T=
ENST00000679443.1:n.821T=
ENST00000679782.1:c.752T=	ENSP00000505995.1:p.Met251=
ENST00000679919.1:n.821T=
ENST00000679928.1:c.*363T=	ENSP00000506071.1:n.*363T=
ENST00000680528.1:n.777T=
ENST00000680999.1:c.752T=	ENSP00000504984.1:p.Met251=
ENST00000681282.1:c.781T=	ENSP00000506339.1:p.Ter261=
ENST00000333213.10:c.752T=	ENSP00000327487.6:p.Met251=
ENST00000578415.1:c.712T=
ENST00000583173.5:c.459-174T=	ENSP00000463619.1:n.459-174T=
ENST00000583818.1:c.701T=	ENSP00000461928.1:n.701T=
NM_207346.2:c.752T=	NP_997229.2:p.Met251=
XM_005257229.2:c.752T=	XP_005257286.1:p.Met251=
XM_006721821.2:c.449T=	XP_006721884.1:p.Met150=
XM_011524616.1:c.752T=	XP_011522918.1:p.Met251=
XM_011524617.1:c.752T=	XP_011522919.1:p.Met251=
XM_011524618.1:c.752T=	XP_011522920.1:p.Met251=
XR_243646.2:n.782T=
XM_005257229.4:c.752T=	XP_005257286.1:p.Met251=
XR_243646.4:n.788T=
NM_207346.3:c.752T= MANE Select	NP_997229.2:p.Met251=