Canonical Allele Identifier: CA2836886585

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516658_75516659insGCC , CM000679.2:g.75516658_75516659insGCC	GRCh38
NC_000017.10:g.73512739_73512740insGCC , CM000679.1:g.73512739_73512740insGCC	GRCh37
NC_000017.9:g.71024334_71024335insGCC	NCBI36
NG_013041.1:g.5131_5132insGCC
NG_033152.1:g.3925_3926insGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.56+42_56+43insGCC MANE Select	ENSP00000327487.6:n.56+42_56+43insGCC
ENST00000434205.8:c.-83+272_-83+273insGCC	ENSP00000406559.4:n.-83+272_-83+273insGCC
ENST00000545228.3:c.56+42_56+43insGCC	ENSP00000438169.3:n.56+42_56+43insGCC
ENST00000579449.2:n.20+42_20+43insGCC
ENST00000580013.6:n.65+42_65+43insGCC
ENST00000583818.2:c.56+42_56+43insGCC	ENSP00000461928.2:n.56+42_56+43insGCC
ENST00000679370.1:n.444-88_444-87insGCC
ENST00000679429.1:c.56+42_56+43insGCC	ENSP00000505403.1:n.56+42_56+43insGCC
ENST00000679782.1:c.56+42_56+43insGCC	ENSP00000505995.1:n.56+42_56+43insGCC
ENST00000679928.1:c.56+42_56+43insGCC	ENSP00000506071.1:n.56+42_56+43insGCC
ENST00000680528.1:n.81+42_81+43insGCC
ENST00000680999.1:c.56+42_56+43insGCC	ENSP00000504984.1:n.56+42_56+43insGCC
ENST00000681282.1:c.56+42_56+43insGCC	ENSP00000506339.1:n.56+42_56+43insGCC
ENST00000333213.10:c.56+42_56+43insGCC	ENSP00000327487.6:n.56+42_56+43insGCC
ENST00000434205.7:c.-83+272_-83+273insGCC	ENSP00000406559.3:n.-83+272_-83+273insGCC
ENST00000580013.5:n.81+42_81+43insGCC
ENST00000583173.5:c.56+42_56+43insGCC	ENSP00000463619.1:n.56+42_56+43insGCC
ENST00000583454.1:n.91+42_91+43insGCC
NM_207346.2:c.56+42_56+43insGCC	NP_997229.2:n.56+42_56+43insGCC
XM_005257229.2:c.56+42_56+43insGCC	XP_005257286.1:n.56+42_56+43insGCC
XM_006721821.2:c.-247-88_-247-87insGCC	XP_006721884.1:n.-247-88_-247-87insGCC
XM_011524616.1:c.56+42_56+43insGCC	XP_011522918.1:n.56+42_56+43insGCC
XM_011524617.1:c.56+42_56+43insGCC	XP_011522919.1:n.56+42_56+43insGCC
XM_011524618.1:c.56+42_56+43insGCC	XP_011522920.1:n.56+42_56+43insGCC
XR_243646.2:n.86+42_86+43insGCC
XM_005257229.4:c.56+42_56+43insGCC	XP_005257286.1:n.56+42_56+43insGCC
XR_243646.4:n.92+42_92+43insGCC
NM_207346.3:c.56+42_56+43insGCC MANE Select	NP_997229.2:n.56+42_56+43insGCC