Canonical Allele Identifier: CA2635893835

Gene: WRAP53

Linked Data

• gnomAD v4: 17-7688421-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7688421G>T , CM000679.2:g.7688421G>T	GRCh38
NC_000017.10:g.7591739G>T , CM000679.1:g.7591739G>T	GRCh37
NC_000017.9:g.7532464G>T	NCBI36
NG_017013.2:g.4130C>A , LRG_321:g.4130C>A
NG_028245.1:g.7351G>T , LRG_375:g.7351G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.-142G>T	ENSP00000513904.1:n.-142G>T
ENST00000316024.9:c.-228G>T	ENSP00000324203.5:n.-228G>T
ENST00000396463.6:c.-142G>T	ENSP00000379727.2:n.-142G>T
ENST00000431639.6:c.-1-227G>T	ENSP00000397219.2:n.-1-227G>T
ENST00000457584.6:c.-1-227G>T	ENSP00000411061.2:n.-1-227G>T
ENST00000498311.5:c.-142G>T	ENSP00000432991.1:n.-142G>T
NM_001143990.1:c.-1-227G>T	NP_001137462.1:n.-1-227G>T
NM_001143991.1:c.-1-227G>T	NP_001137463.1:n.-1-227G>T
NM_001143992.1:c.-142G>T	NP_001137464.1:n.-142G>T
NM_018081.2:c.-228G>T , LRG_375t1:c.-228G>T	NP_060551.2:n.-228G>T
XM_024450825.1:c.-142G>T	XP_024306593.1:n.-142G>T
XR_001752551.2:n.104G>T
NM_001143991.2:c.-1-227G>T	NP_001137463.1:n.-1-227G>T
NM_001143990.2:c.-1-227G>T	NP_001137462.1:n.-1-227G>T