Canonical Allele Identifier: CA2245953228

Gene: WRAP53

Linked Data

• dbSNP Id: rs2074049143

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7688458_7688474del , CM000679.2:g.7688458_7688474del	GRCh38
NC_000017.10:g.7591776_7591792del , CM000679.1:g.7591776_7591792del	GRCh37
NC_000017.9:g.7532501_7532517del	NCBI36
NG_017013.2:g.4079_4095del , LRG_321:g.4079_4095del
NG_028245.1:g.7388_7404del , LRG_375:g.7388_7404del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.-105_-89del	ENSP00000513904.1:n.-105_-89del
ENST00000698743.1:c.-105_-89del	ENSP00000513905.1:n.-105_-89del
ENST00000316024.9:c.-191_-175del	ENSP00000324203.5:n.-191_-175del
ENST00000396463.6:c.-105_-89del	ENSP00000379727.2:n.-105_-89del
ENST00000431639.6:c.-1-190_-1-174del	ENSP00000397219.2:n.-1-190_-1-174del
ENST00000457584.6:c.-1-190_-1-174del	ENSP00000411061.2:n.-1-190_-1-174del
ENST00000498311.5:c.-105_-89del	ENSP00000432991.1:n.-105_-89del
NM_001143990.1:c.-1-190_-1-174del	NP_001137462.1:n.-1-190_-1-174del
NM_001143991.1:c.-1-190_-1-174del	NP_001137463.1:n.-1-190_-1-174del
NM_001143992.1:c.-105_-89del	NP_001137464.1:n.-105_-89del
NM_018081.2:c.-191_-175del , LRG_375t1:c.-191_-175del	NP_060551.2:n.-191_-175del
XM_024450825.1:c.-105_-89del	XP_024306593.1:n.-105_-89del
XR_001752551.2:n.141_157del
NM_001143991.2:c.-1-190_-1-174del	NP_001137463.1:n.-1-190_-1-174del
NM_001143990.2:c.-1-190_-1-174del	NP_001137462.1:n.-1-190_-1-174del