Canonical Allele Identifier: CA2573154899

Gene: TSEN54

Linked Data

• ClinVar Variation Id: 1395769
• ClinVar RCV Id: RCV001901254
• dbSNP Id: rs2147005509

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516792dup , CM000679.2:g.75516792dup	GRCh38
NC_000017.10:g.73512873dup , CM000679.1:g.73512873dup	GRCh37
NC_000017.9:g.71024468dup	NCBI36
NG_013041.1:g.5265dup
NG_033152.1:g.3795dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.103dup MANE Select	ENSP00000327487.6:p.Gln35ProfsTer?
ENST00000434205.8:c.-82-217dup	ENSP00000406559.4:n.-82-217dup
ENST00000545228.3:c.103dup	ENSP00000438169.3:p.Gln35ProfsTer?
ENST00000579449.2:n.20+176dup
ENST00000580013.6:n.112dup
ENST00000583818.2:c.103dup	ENSP00000461928.2:p.Gln35ProfsTer?
ENST00000679370.1:n.490dup
ENST00000679429.1:c.103dup	ENSP00000505403.1:p.Gln35ProfsTer?
ENST00000679782.1:c.103dup	ENSP00000505995.1:p.Gln35ProfsTer?
ENST00000679928.1:c.103dup	ENSP00000506071.1:p.Gln35ProfsTer?
ENST00000680528.1:n.128dup
ENST00000680999.1:c.103dup	ENSP00000504984.1:p.Gln35ProfsTer?
ENST00000681282.1:c.103dup	ENSP00000506339.1:p.Gln35ProfsTer?
ENST00000333213.10:c.103dup	ENSP00000327487.6:p.Gln35ProfsTer?
ENST00000434205.7:c.-82-217dup	ENSP00000406559.3:n.-82-217dup
ENST00000580013.5:n.128dup
ENST00000583173.5:c.56+176dup	ENSP00000463619.1:n.56+176dup
ENST00000583454.1:n.138dup
NM_207346.2:c.103dup	NP_997229.2:p.Gln35ProfsTer?
XM_005257229.2:c.103dup	XP_005257286.1:p.Gln35ProfsTer?
XM_006721821.2:c.-201dup	XP_006721884.1:n.-201dup
XM_011524616.1:c.103dup	XP_011522918.1:p.Gln35ProfsTer?
XM_011524617.1:c.103dup	XP_011522919.1:p.Gln35ProfsTer?
XM_011524618.1:c.103dup	XP_011522920.1:p.Gln35ProfsTer?
XR_243646.2:n.133dup
XM_005257229.4:c.103dup	XP_005257286.1:p.Gln35ProfsTer?
XR_243646.4:n.139dup
NM_207346.3:c.103dup MANE Select	NP_997229.2:p.Gln35ProfsTer?