Canonical Allele Identifier: CA2275552746

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524664_75524666delinsCTG , CM000679.2:g.75524664_75524666delinsCTG	GRCh38
NC_000017.10:g.73520745_73520747delinsCTG , CM000679.1:g.73520745_73520747delinsCTG	GRCh37
NC_000017.9:g.71032340_71032342delinsCTG	NCBI36
NG_013041.1:g.13137_13139delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*252_*254delinsCTG MANE Select	ENSP00000327487.6:n.*252_*254delinsCTG
ENST00000434205.8:c.*252_*254delinsCTG	ENSP00000406559.4:n.*252_*254delinsCTG
ENST00000545228.3:c.*332_*334delinsCTG	ENSP00000438169.3:n.*332_*334delinsCTG
ENST00000577197.2:n.1031_1033delinsCTG
ENST00000579449.2:n.2573_2575delinsCTG
ENST00000580013.6:n.2977_2979delinsCTG
ENST00000679370.1:n.3355_3357delinsCTG
ENST00000679429.1:c.*1291_*1293delinsCTG	ENSP00000505403.1:n.*1291_*1293delinsCTG
ENST00000679443.1:n.1902_1904delinsCTG
ENST00000679782.1:c.*532_*534delinsCTG	ENSP00000505995.1:n.*532_*534delinsCTG
ENST00000679919.1:n.2104_2106delinsCTG
ENST00000679928.1:c.*2385_*2387delinsCTG	ENSP00000506071.1:n.*2385_*2387delinsCTG
ENST00000680999.1:c.*252_*254delinsCTG	ENSP00000504984.1:n.*252_*254delinsCTG
ENST00000681282.1:c.*2020_*2022delinsCTG	ENSP00000506339.1:n.*2020_*2022delinsCTG
ENST00000333213.10:c.*252_*254delinsCTG	ENSP00000327487.6:n.*252_*254delinsCTG
ENST00000545228.2:c.1110_1112delinsCTG
ENST00000577197.1:n.581_583delinsCTG
NM_207346.2:c.*252_*254delinsCTG	NP_997229.2:n.*252_*254delinsCTG
XM_005257229.2:c.*332_*334delinsCTG	XP_005257286.1:n.*332_*334delinsCTG
XM_006721821.2:c.*332_*334delinsCTG	XP_006721884.1:n.*332_*334delinsCTG
XM_011524616.1:c.*332_*334delinsCTG	XP_011522918.1:n.*332_*334delinsCTG
XM_011524618.1:c.*252_*254delinsCTG	XP_011522920.1:n.*252_*254delinsCTG
XR_243646.2:n.2065_2067delinsCTG
XM_005257229.4:c.*332_*334delinsCTG	XP_005257286.1:n.*332_*334delinsCTG
XR_243646.4:n.2071_2073delinsCTG
NM_207346.3:c.*252_*254delinsCTG MANE Select	NP_997229.2:n.*252_*254delinsCTG