Canonical Allele Identifier: CA2275548296

Gene: TSEN54

Linked Data

• dbSNP Id: rs2053367201

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516541dup , CM000679.2:g.75516541dup	GRCh38
NC_000017.10:g.73512622dup , CM000679.1:g.73512622dup	GRCh37
NC_000017.9:g.71024217dup	NCBI36
NG_013041.1:g.5014dup
NG_033152.1:g.4043dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.-20dup MANE Select	ENSP00000327487.6:n.-20dup
ENST00000434205.8:c.-83+155dup	ENSP00000406559.4:n.-83+155dup
ENST00000679370.1:n.443+155dup
ENST00000679429.1:c.-20dup	ENSP00000505403.1:n.-20dup
ENST00000679928.1:c.-20dup	ENSP00000506071.1:n.-20dup
ENST00000680528.1:n.6dup
ENST00000681282.1:c.-20dup	ENSP00000506339.1:n.-20dup
ENST00000333213.10:c.-20dup	ENSP00000327487.6:n.-20dup
ENST00000434205.7:c.-83+155dup	ENSP00000406559.3:n.-83+155dup
ENST00000580013.5:n.6dup
ENST00000583454.1:n.16dup
NM_207346.2:c.-20dup	NP_997229.2:n.-20dup
XM_005257229.2:c.-20dup	XP_005257286.1:n.-20dup
XM_006721821.2:c.-248+155dup	XP_006721884.1:n.-248+155dup
XM_011524616.1:c.-20dup	XP_011522918.1:n.-20dup
XM_011524617.1:c.-20dup	XP_011522919.1:n.-20dup
XM_011524618.1:c.-20dup	XP_011522920.1:n.-20dup
XR_243646.2:n.11dup
XM_005257229.4:c.-20dup	XP_005257286.1:n.-20dup
XR_243646.4:n.17dup
NM_207346.3:c.-20dup MANE Select	NP_997229.2:n.-20dup