Canonical Allele Identifier: CA2275552663

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524508C= , CM000679.2:g.75524508C=	GRCh38
NC_000017.10:g.73520589C= , CM000679.1:g.73520589C=	GRCh37
NC_000017.9:g.71032184C=	NCBI36
NG_013041.1:g.12981C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*96C= MANE Select	ENSP00000327487.6:n.*96C=
ENST00000434205.8:c.*96C=	ENSP00000406559.4:n.*96C=
ENST00000545228.3:c.*176C=	ENSP00000438169.3:n.*176C=
ENST00000577197.2:n.875C=
ENST00000579449.2:n.2417C=
ENST00000580013.6:n.2821C=
ENST00000679370.1:n.3199C=
ENST00000679429.1:c.*1135C=	ENSP00000505403.1:n.*1135C=
ENST00000679443.1:n.1746C=
ENST00000679782.1:c.*376C=	ENSP00000505995.1:n.*376C=
ENST00000679919.1:n.1948C=
ENST00000679928.1:c.*2229C=	ENSP00000506071.1:n.*2229C=
ENST00000680999.1:c.*96C=	ENSP00000504984.1:n.*96C=
ENST00000681282.1:c.*1864C=	ENSP00000506339.1:n.*1864C=
ENST00000333213.10:c.*96C=	ENSP00000327487.6:n.*96C=
ENST00000545228.2:c.954C=
ENST00000577197.1:n.425C=
NM_207346.2:c.*96C=	NP_997229.2:n.*96C=
XM_005257229.2:c.*176C=	XP_005257286.1:n.*176C=
XM_006721821.2:c.*176C=	XP_006721884.1:n.*176C=
XM_011524616.1:c.*176C=	XP_011522918.1:n.*176C=
XM_011524618.1:c.*96C=	XP_011522920.1:n.*96C=
XR_243646.2:n.1909C=
XM_005257229.4:c.*176C=	XP_005257286.1:n.*176C=
XR_243646.4:n.1915C=
NM_207346.3:c.*96C= MANE Select	NP_997229.2:n.*96C=