Canonical Allele Identifier: CA2275551346

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521997A= , CM000679.2:g.75521997A=	GRCh38
NC_000017.10:g.73518078A= , CM000679.1:g.73518078A=	GRCh37
NC_000017.9:g.71029673A=	NCBI36
NG_013041.1:g.10470A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.916A= MANE Select	ENSP00000327487.6:p.Met306=
ENST00000434205.8:c.613A=	ENSP00000406559.4:p.Met205=
ENST00000545228.3:c.916A=	ENSP00000438169.3:p.Met306=
ENST00000579449.2:n.715A=
ENST00000580013.6:n.1119A=
ENST00000679370.1:n.1497A=
ENST00000679429.1:c.*374A=	ENSP00000505403.1:n.*374A=
ENST00000679443.1:n.985A=
ENST00000679782.1:c.916A=	ENSP00000505995.1:p.Met306=
ENST00000679919.1:n.985A=
ENST00000679928.1:c.*527A=	ENSP00000506071.1:n.*527A=
ENST00000680528.1:n.941A=
ENST00000680999.1:c.916A=	ENSP00000504984.1:p.Met306=
ENST00000681282.1:c.*162A=	ENSP00000506339.1:n.*162A=
ENST00000333213.10:c.916A=	ENSP00000327487.6:p.Met306=
ENST00000545228.2:c.5A=
ENST00000578415.1:c.876A=
ENST00000583173.5:c.459-10A=	ENSP00000463619.1:n.459-10A=
NM_207346.2:c.916A=	NP_997229.2:p.Met306=
XM_005257229.2:c.916A=	XP_005257286.1:p.Met306=
XM_006721821.2:c.613A=	XP_006721884.1:p.Met205=
XM_011524616.1:c.916A=	XP_011522918.1:p.Met306=
XM_011524617.1:c.916A=	XP_011522919.1:p.Met306=
XM_011524618.1:c.916A=	XP_011522920.1:p.Met306=
XR_243646.2:n.946A=
XM_005257229.4:c.916A=	XP_005257286.1:p.Met306=
XR_243646.4:n.952A=
NM_207346.3:c.916A= MANE Select	NP_997229.2:p.Met306=