Canonical Allele Identifier: CA2275549651

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75518922_75518924delinsCTG , CM000679.2:g.75518922_75518924delinsCTG	GRCh38
NC_000017.10:g.73515003_73515005delinsCTG , CM000679.1:g.73515003_73515005delinsCTG	GRCh37
NC_000017.9:g.71026598_71026600delinsCTG	NCBI36
NG_013041.1:g.7395_7397delinsCTG
NG_033152.1:g.1660_1662delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.469-73_469-71delinsCTG MANE Select	ENSP00000327487.6:n.469-73_469-71delinsCTG
ENST00000434205.8:c.166-73_166-71delinsCTG	ENSP00000406559.4:n.166-73_166-71delinsCTG
ENST00000545228.3:c.469-73_469-71delinsCTG	ENSP00000438169.3:n.469-73_469-71delinsCTG
ENST00000579449.2:n.268-73_268-71delinsCTG
ENST00000580013.6:n.478-73_478-71delinsCTG
ENST00000583818.2:c.469-73_469-71delinsCTG	ENSP00000461928.2:n.469-73_469-71delinsCTG
ENST00000679370.1:n.856-73_856-71delinsCTG
ENST00000679429.1:c.469-81_469-79delinsCTG	ENSP00000505403.1:n.469-81_469-79delinsCTG
ENST00000679443.1:n.344-73_344-71delinsCTG
ENST00000679782.1:c.469-73_469-71delinsCTG	ENSP00000505995.1:n.469-73_469-71delinsCTG
ENST00000679919.1:n.344-73_344-71delinsCTG
ENST00000679928.1:c.469-73_469-71delinsCTG	ENSP00000506071.1:n.469-73_469-71delinsCTG
ENST00000680528.1:n.494-73_494-71delinsCTG
ENST00000680999.1:c.469-73_469-71delinsCTG	ENSP00000504984.1:n.469-73_469-71delinsCTG
ENST00000681282.1:c.469-73_469-71delinsCTG	ENSP00000506339.1:n.469-73_469-71delinsCTG
ENST00000333213.10:c.469-73_469-71delinsCTG	ENSP00000327487.6:n.469-73_469-71delinsCTG
ENST00000434205.7:c.166-73_166-71delinsCTG	ENSP00000406559.3:n.166-73_166-71delinsCTG
ENST00000578415.1:c.429-73_429-71delinsCTG
ENST00000580013.5:n.494-81_494-79delinsCTG
ENST00000583173.5:c.304-73_304-71delinsCTG	ENSP00000463619.1:n.304-73_304-71delinsCTG
ENST00000583818.1:c.364-73_364-71delinsCTG	ENSP00000461928.1:n.364-73_364-71delinsCTG
NM_207346.2:c.469-73_469-71delinsCTG	NP_997229.2:n.469-73_469-71delinsCTG
XM_005257229.2:c.469-73_469-71delinsCTG	XP_005257286.1:n.469-73_469-71delinsCTG
XM_006721821.2:c.166-73_166-71delinsCTG	XP_006721884.1:n.166-73_166-71delinsCTG
XM_011524616.1:c.469-73_469-71delinsCTG	XP_011522918.1:n.469-73_469-71delinsCTG
XM_011524617.1:c.469-73_469-71delinsCTG	XP_011522919.1:n.469-73_469-71delinsCTG
XM_011524618.1:c.469-73_469-71delinsCTG	XP_011522920.1:n.469-73_469-71delinsCTG
XR_243646.2:n.499-73_499-71delinsCTG
XM_005257229.4:c.469-73_469-71delinsCTG	XP_005257286.1:n.469-73_469-71delinsCTG
XR_243646.4:n.505-73_505-71delinsCTG
NM_207346.3:c.469-73_469-71delinsCTG MANE Select	NP_997229.2:n.469-73_469-71delinsCTG