Canonical Allele Identifier: CA2635894004

Gene: WRAP53

Linked Data

• dbSNP Id: rs2151084330
• gnomAD v4: 17-7688545-AGAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7688550_7688552del , CM000679.2:g.7688550_7688552del	GRCh38
NC_000017.10:g.7591868_7591870del , CM000679.1:g.7591868_7591870del	GRCh37
NC_000017.9:g.7532593_7532595del	NCBI36
NG_017013.2:g.4003_4005del , LRG_321:g.4003_4005del
NG_028245.1:g.7480_7482del , LRG_375:g.7480_7482del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.-13_-11del	ENSP00000513904.1:n.-13_-11del
ENST00000698743.1:c.-13_-11del	ENSP00000513905.1:n.-13_-11del
ENST00000698744.1:c.-13_-11del	ENSP00000513906.1:n.-13_-11del
ENST00000698745.1:c.-13_-11del	ENSP00000513907.1:n.-13_-11del
ENST00000698746.1:c.-13_-11del	ENSP00000513908.1:n.-13_-11del
ENST00000396463.7:c.-13_-11del MANE Select	ENSP00000379727.3:n.-13_-11del
ENST00000316024.9:c.-99_-97del	ENSP00000324203.5:n.-99_-97del
ENST00000396463.6:c.-13_-11del	ENSP00000379727.2:n.-13_-11del
ENST00000431639.6:c.-1-98_-1-96del	ENSP00000397219.2:n.-1-98_-1-96del
ENST00000457584.6:c.-1-98_-1-96del	ENSP00000411061.2:n.-1-98_-1-96del
ENST00000467699.5:n.74_76del
ENST00000498311.5:c.-13_-11del	ENSP00000432991.1:n.-13_-11del
ENST00000534050.5:c.-99_-97del	ENSP00000434999.1:n.-99_-97del
NM_001143990.1:c.-1-98_-1-96del	NP_001137462.1:n.-1-98_-1-96del
NM_001143991.1:c.-1-98_-1-96del	NP_001137463.1:n.-1-98_-1-96del
NM_001143992.1:c.-13_-11del	NP_001137464.1:n.-13_-11del
NM_018081.2:c.-99_-97del , LRG_375t1:c.-99_-97del	NP_060551.2:n.-99_-97del
XM_024450824.1:c.-2088_-2086del	XP_024306592.1:n.-2088_-2086del
XM_024450825.1:c.-13_-11del	XP_024306593.1:n.-13_-11del
XR_001752551.2:n.233_235del
NM_001143991.2:c.-1-98_-1-96del	NP_001137463.1:n.-1-98_-1-96del
NM_001143992.2:c.-13_-11del MANE Select	NP_001137464.1:n.-13_-11del
NM_001143990.2:c.-1-98_-1-96del	NP_001137462.1:n.-1-98_-1-96del