Canonical Allele Identifier: CA2576388792

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521365_75521369dup , CM000679.2:g.75521365_75521369dup	GRCh38
NC_000017.10:g.73517446_73517450dup , CM000679.1:g.73517446_73517450dup	GRCh37
NC_000017.9:g.71029041_71029045dup	NCBI36
NG_013041.1:g.9838_9842dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.522-44_522-40dup MANE Select	ENSP00000327487.6:n.522-44_522-40dup
ENST00000434205.8:c.219-44_219-40dup	ENSP00000406559.4:n.219-44_219-40dup
ENST00000545228.3:c.522-44_522-40dup	ENSP00000438169.3:n.522-44_522-40dup
ENST00000579449.2:n.321-44_321-40dup
ENST00000580013.6:n.531-44_531-40dup
ENST00000583818.2:c.532_536dup	ENSP00000461928.2:n.532_536dup
ENST00000679370.1:n.909-44_909-40dup
ENST00000679429.1:c.514-44_514-40dup	ENSP00000505403.1:n.514-44_514-40dup
ENST00000679443.1:n.397-44_397-40dup
ENST00000679782.1:c.522-44_522-40dup	ENSP00000505995.1:n.522-44_522-40dup
ENST00000679919.1:n.397-44_397-40dup
ENST00000679928.1:c.*133-44_*133-40dup	ENSP00000506071.1:n.*133-44_*133-40dup
ENST00000680528.1:n.547-44_547-40dup
ENST00000680999.1:c.522-44_522-40dup	ENSP00000504984.1:n.522-44_522-40dup
ENST00000681282.1:c.522-44_522-40dup	ENSP00000506339.1:n.522-44_522-40dup
ENST00000333213.10:c.522-44_522-40dup	ENSP00000327487.6:n.522-44_522-40dup
ENST00000578415.1:c.482-44_482-40dup
ENST00000580013.5:n.539-44_539-40dup
ENST00000583173.5:c.357-44_357-40dup	ENSP00000463619.1:n.357-44_357-40dup
ENST00000583818.1:c.427_431dup	ENSP00000461928.1:n.427_431dup
NM_207346.2:c.522-44_522-40dup	NP_997229.2:n.522-44_522-40dup
XM_005257229.2:c.522-44_522-40dup	XP_005257286.1:n.522-44_522-40dup
XM_006721821.2:c.219-44_219-40dup	XP_006721884.1:n.219-44_219-40dup
XM_011524616.1:c.522-44_522-40dup	XP_011522918.1:n.522-44_522-40dup
XM_011524617.1:c.522-44_522-40dup	XP_011522919.1:n.522-44_522-40dup
XM_011524618.1:c.522-44_522-40dup	XP_011522920.1:n.522-44_522-40dup
XR_243646.2:n.552-44_552-40dup
XM_005257229.4:c.522-44_522-40dup	XP_005257286.1:n.522-44_522-40dup
XR_243646.4:n.558-44_558-40dup
NM_207346.3:c.522-44_522-40dup MANE Select	NP_997229.2:n.522-44_522-40dup