Canonical Allele Identifier: CA2635893980

Gene: WRAP53

Linked Data

• gnomAD v4: 17-7688528-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7688528T>G , CM000679.2:g.7688528T>G	GRCh38
NC_000017.10:g.7591846T>G , CM000679.1:g.7591846T>G	GRCh37
NC_000017.9:g.7532571T>G	NCBI36
NG_017013.2:g.4023A>C , LRG_321:g.4023A>C
NG_028245.1:g.7458T>G , LRG_375:g.7458T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.-35T>G	ENSP00000513904.1:n.-35T>G
ENST00000698743.1:c.-35T>G	ENSP00000513905.1:n.-35T>G
ENST00000698744.1:c.-35T>G	ENSP00000513906.1:n.-35T>G
ENST00000698745.1:c.-35T>G	ENSP00000513907.1:n.-35T>G
ENST00000698746.1:c.-35T>G	ENSP00000513908.1:n.-35T>G
ENST00000396463.7:c.-35T>G MANE Select	ENSP00000379727.3:n.-35T>G
ENST00000316024.9:c.-121T>G	ENSP00000324203.5:n.-121T>G
ENST00000396463.6:c.-35T>G	ENSP00000379727.2:n.-35T>G
ENST00000431639.6:c.-1-120T>G	ENSP00000397219.2:n.-1-120T>G
ENST00000457584.6:c.-1-120T>G	ENSP00000411061.2:n.-1-120T>G
ENST00000467699.5:n.52T>G
ENST00000498311.5:c.-35T>G	ENSP00000432991.1:n.-35T>G
ENST00000534050.5:c.-121T>G	ENSP00000434999.1:n.-121T>G
NM_001143990.1:c.-1-120T>G	NP_001137462.1:n.-1-120T>G
NM_001143991.1:c.-1-120T>G	NP_001137463.1:n.-1-120T>G
NM_001143992.1:c.-35T>G	NP_001137464.1:n.-35T>G
NM_018081.2:c.-121T>G , LRG_375t1:c.-121T>G	NP_060551.2:n.-121T>G
XM_024450824.1:c.-2110T>G	XP_024306592.1:n.-2110T>G
XM_024450825.1:c.-35T>G	XP_024306593.1:n.-35T>G
XR_001752551.2:n.211T>G
NM_001143991.2:c.-1-120T>G	NP_001137463.1:n.-1-120T>G
NM_001143992.2:c.-35T>G MANE Select	NP_001137464.1:n.-35T>G
NM_001143990.2:c.-1-120T>G	NP_001137462.1:n.-1-120T>G