Canonical Allele Identifier: CA2275551377

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75522045C= , CM000679.2:g.75522045C=	GRCh38
NC_000017.10:g.73518126C= , CM000679.1:g.73518126C=	GRCh37
NC_000017.9:g.71029721C=	NCBI36
NG_013041.1:g.10518C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.964C= MANE Select	ENSP00000327487.6:p.Leu322=
ENST00000434205.8:c.661C=	ENSP00000406559.4:p.Leu221=
ENST00000545228.3:c.964C=	ENSP00000438169.3:p.Leu322=
ENST00000579449.2:n.763C=
ENST00000580013.6:n.1167C=
ENST00000679370.1:n.1545C=
ENST00000679429.1:c.*422C=	ENSP00000505403.1:n.*422C=
ENST00000679443.1:n.1033C=
ENST00000679782.1:c.964C=	ENSP00000505995.1:p.Leu322=
ENST00000679919.1:n.1033C=
ENST00000679928.1:c.*575C=	ENSP00000506071.1:n.*575C=
ENST00000680528.1:n.989C=
ENST00000680999.1:c.964C=	ENSP00000504984.1:p.Leu322=
ENST00000681282.1:c.*210C=	ENSP00000506339.1:n.*210C=
ENST00000333213.10:c.964C=	ENSP00000327487.6:p.Leu322=
ENST00000545228.2:c.53C=
ENST00000578415.1:c.924C=
ENST00000583173.5:c.497C=	ENSP00000463619.1:p.Ala166=
NM_207346.2:c.964C=	NP_997229.2:p.Leu322=
XM_005257229.2:c.964C=	XP_005257286.1:p.Leu322=
XM_006721821.2:c.661C=	XP_006721884.1:p.Leu221=
XM_011524616.1:c.964C=	XP_011522918.1:p.Leu322=
XM_011524617.1:c.964C=	XP_011522919.1:p.Leu322=
XM_011524618.1:c.964C=	XP_011522920.1:p.Leu322=
XR_243646.2:n.994C=
XM_005257229.4:c.964C=	XP_005257286.1:p.Leu322=
XR_243646.4:n.1000C=
NM_207346.3:c.964C= MANE Select	NP_997229.2:p.Leu322=