Canonical Allele Identifier: CA2832572169

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516539_75516631del , CM000679.2:g.75516539_75516631del	GRCh38
NC_000017.10:g.73512620_73512712del , CM000679.1:g.73512620_73512712del	GRCh37
NC_000017.9:g.71024215_71024307del	NCBI36
NG_013041.1:g.5012_5104del
NG_033152.1:g.3955_4047del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.-22_56+15del
ENST00000434205.8:c.-83+153_-83+245del	ENSP00000406559.4:n.-83+153_-83+245del
ENST00000679370.1:n.443+153_444-115del
ENST00000679429.1:c.-22_56+15del
ENST00000679928.1:c.-22_56+15del
ENST00000680528.1:n.4_81+15del
ENST00000681282.1:c.-22_56+15del
ENST00000333213.10:c.-22_56+15del
ENST00000434205.7:c.-83+153_-83+245del	ENSP00000406559.3:n.-83+153_-83+245del
ENST00000580013.5:n.4_81+15del
ENST00000583454.1:n.14_91+15del
NM_207346.2:c.-22_56+15del
XM_005257229.2:c.-22_56+15del
XM_006721821.2:c.-248+153_-247-115del	XP_006721884.1:n.-248+153_-247-115del
XM_011524616.1:c.-22_56+15del
XM_011524617.1:c.-22_56+15del
XM_011524618.1:c.-22_56+15del
XR_243646.2:n.9_86+15del
XM_005257229.4:c.-22_56+15del
XR_243646.4:n.15_92+15del
NM_207346.3:c.-22_56+15del