Canonical Allele Identifier: CA2639835882

Gene: TSEN54

Linked Data

• gnomAD v4: 17-75516630-C-CGGCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516632_75516636dup , CM000679.2:g.75516632_75516636dup	GRCh38
NC_000017.10:g.73512713_73512717dup , CM000679.1:g.73512713_73512717dup	GRCh37
NC_000017.9:g.71024308_71024312dup	NCBI36
NG_013041.1:g.5105_5109dup
NG_033152.1:g.3949_3953dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.56+16_56+20dup MANE Select	ENSP00000327487.6:n.56+16_56+20dup
ENST00000434205.8:c.-83+246_-83+250dup	ENSP00000406559.4:n.-83+246_-83+250dup
ENST00000545228.3:c.56+16_56+20dup	ENSP00000438169.3:n.56+16_56+20dup
ENST00000579449.2:n.20+16_20+20dup
ENST00000580013.6:n.65+16_65+20dup
ENST00000583818.2:c.56+16_56+20dup	ENSP00000461928.2:n.56+16_56+20dup
ENST00000679370.1:n.444-114_444-110dup
ENST00000679429.1:c.56+16_56+20dup	ENSP00000505403.1:n.56+16_56+20dup
ENST00000679782.1:c.56+16_56+20dup	ENSP00000505995.1:n.56+16_56+20dup
ENST00000679928.1:c.56+16_56+20dup	ENSP00000506071.1:n.56+16_56+20dup
ENST00000680528.1:n.81+16_81+20dup
ENST00000680999.1:c.56+16_56+20dup	ENSP00000504984.1:n.56+16_56+20dup
ENST00000681282.1:c.56+16_56+20dup	ENSP00000506339.1:n.56+16_56+20dup
ENST00000333213.10:c.56+16_56+20dup	ENSP00000327487.6:n.56+16_56+20dup
ENST00000434205.7:c.-83+246_-83+250dup	ENSP00000406559.3:n.-83+246_-83+250dup
ENST00000580013.5:n.81+16_81+20dup
ENST00000583173.5:c.56+16_56+20dup	ENSP00000463619.1:n.56+16_56+20dup
ENST00000583454.1:n.91+16_91+20dup
NM_207346.2:c.56+16_56+20dup	NP_997229.2:n.56+16_56+20dup
XM_005257229.2:c.56+16_56+20dup	XP_005257286.1:n.56+16_56+20dup
XM_006721821.2:c.-247-114_-247-110dup	XP_006721884.1:n.-247-114_-247-110dup
XM_011524616.1:c.56+16_56+20dup	XP_011522918.1:n.56+16_56+20dup
XM_011524617.1:c.56+16_56+20dup	XP_011522919.1:n.56+16_56+20dup
XM_011524618.1:c.56+16_56+20dup	XP_011522920.1:n.56+16_56+20dup
XR_243646.2:n.86+16_86+20dup
XM_005257229.4:c.56+16_56+20dup	XP_005257286.1:n.56+16_56+20dup
XR_243646.4:n.92+16_92+20dup
NM_207346.3:c.56+16_56+20dup MANE Select	NP_997229.2:n.56+16_56+20dup