Canonical Allele Identifier: CA2275552762

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524689C= , CM000679.2:g.75524689C=	GRCh38
NC_000017.10:g.73520770C= , CM000679.1:g.73520770C=	GRCh37
NC_000017.9:g.71032365C=	NCBI36
NG_013041.1:g.13162C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*277C= MANE Select	ENSP00000327487.6:n.*277C=
ENST00000434205.8:c.*277C=	ENSP00000406559.4:n.*277C=
ENST00000545228.3:c.*357C=	ENSP00000438169.3:n.*357C=
ENST00000577197.2:n.1056C=
ENST00000579449.2:n.2598C=
ENST00000580013.6:n.3002C=
ENST00000679370.1:n.3380C=
ENST00000679429.1:c.*1316C=	ENSP00000505403.1:n.*1316C=
ENST00000679443.1:n.1927C=
ENST00000679782.1:c.*557C=	ENSP00000505995.1:n.*557C=
ENST00000679919.1:n.2129C=
ENST00000679928.1:c.*2410C=	ENSP00000506071.1:n.*2410C=
ENST00000680999.1:c.*277C=	ENSP00000504984.1:n.*277C=
ENST00000681282.1:c.*2045C=	ENSP00000506339.1:n.*2045C=
ENST00000333213.10:c.*277C=	ENSP00000327487.6:n.*277C=
ENST00000545228.2:c.1135C=
ENST00000577197.1:n.606C=
NM_207346.2:c.*277C=	NP_997229.2:n.*277C=
XM_005257229.2:c.*357C=	XP_005257286.1:n.*357C=
XM_006721821.2:c.*357C=	XP_006721884.1:n.*357C=
XM_011524616.1:c.*357C=	XP_011522918.1:n.*357C=
XM_011524618.1:c.*277C=	XP_011522920.1:n.*277C=
XR_243646.2:n.2090C=
XM_005257229.4:c.*357C=	XP_005257286.1:n.*357C=
XR_243646.4:n.2096C=
NM_207346.3:c.*277C= MANE Select	NP_997229.2:n.*277C=