Canonical Allele Identifier: CA2739561862

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524495A>G , CM000679.2:g.75524495A>G	GRCh38
NC_000017.10:g.73520576A>G , CM000679.1:g.73520576A>G	GRCh37
NC_000017.9:g.71032171A>G	NCBI36
NG_013041.1:g.12968A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*83A>G MANE Select	ENSP00000327487.6:n.*83A>G
ENST00000434205.8:c.*83A>G	ENSP00000406559.4:n.*83A>G
ENST00000545228.3:c.*163A>G	ENSP00000438169.3:n.*163A>G
ENST00000577197.2:n.862A>G
ENST00000579449.2:n.2404A>G
ENST00000580013.6:n.2808A>G
ENST00000679370.1:n.3186A>G
ENST00000679429.1:c.*1122A>G	ENSP00000505403.1:n.*1122A>G
ENST00000679443.1:n.1733A>G
ENST00000679782.1:c.*363A>G	ENSP00000505995.1:n.*363A>G
ENST00000679919.1:n.1935A>G
ENST00000679928.1:c.*2216A>G	ENSP00000506071.1:n.*2216A>G
ENST00000680999.1:c.*83A>G	ENSP00000504984.1:n.*83A>G
ENST00000681282.1:c.*1851A>G	ENSP00000506339.1:n.*1851A>G
ENST00000333213.10:c.*83A>G	ENSP00000327487.6:n.*83A>G
ENST00000545228.2:c.941A>G
ENST00000577197.1:n.412A>G
NM_207346.2:c.*83A>G	NP_997229.2:n.*83A>G
XM_005257229.2:c.*163A>G	XP_005257286.1:n.*163A>G
XM_006721821.2:c.*163A>G	XP_006721884.1:n.*163A>G
XM_011524616.1:c.*163A>G	XP_011522918.1:n.*163A>G
XM_011524618.1:c.*83A>G	XP_011522920.1:n.*83A>G
XR_243646.2:n.1896A>G
XM_005257229.4:c.*163A>G	XP_005257286.1:n.*163A>G
XR_243646.4:n.1902A>G
NM_207346.3:c.*83A>G MANE Select	NP_997229.2:n.*83A>G