Canonical Allele Identifier: CA2275552731

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524636G= , CM000679.2:g.75524636G=	GRCh38
NC_000017.10:g.73520717G= , CM000679.1:g.73520717G=	GRCh37
NC_000017.9:g.71032312G=	NCBI36
NG_013041.1:g.13109G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*224G= MANE Select	ENSP00000327487.6:n.*224G=
ENST00000434205.8:c.*224G=	ENSP00000406559.4:n.*224G=
ENST00000545228.3:c.*304G=	ENSP00000438169.3:n.*304G=
ENST00000577197.2:n.1003G=
ENST00000579449.2:n.2545G=
ENST00000580013.6:n.2949G=
ENST00000679370.1:n.3327G=
ENST00000679429.1:c.*1263G=	ENSP00000505403.1:n.*1263G=
ENST00000679443.1:n.1874G=
ENST00000679782.1:c.*504G=	ENSP00000505995.1:n.*504G=
ENST00000679919.1:n.2076G=
ENST00000679928.1:c.*2357G=	ENSP00000506071.1:n.*2357G=
ENST00000680999.1:c.*224G=	ENSP00000504984.1:n.*224G=
ENST00000681282.1:c.*1992G=	ENSP00000506339.1:n.*1992G=
ENST00000333213.10:c.*224G=	ENSP00000327487.6:n.*224G=
ENST00000545228.2:c.1082G=
ENST00000577197.1:n.553G=
NM_207346.2:c.*224G=	NP_997229.2:n.*224G=
XM_005257229.2:c.*304G=	XP_005257286.1:n.*304G=
XM_006721821.2:c.*304G=	XP_006721884.1:n.*304G=
XM_011524616.1:c.*304G=	XP_011522918.1:n.*304G=
XM_011524618.1:c.*224G=	XP_011522920.1:n.*224G=
XR_243646.2:n.2037G=
XM_005257229.4:c.*304G=	XP_005257286.1:n.*304G=
XR_243646.4:n.2043G=
NM_207346.3:c.*224G= MANE Select	NP_997229.2:n.*224G=