Canonical Allele Identifier: CA2635893838

Gene: WRAP53

Linked Data

• gnomAD v4: 17-7688425-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7688425G>A , CM000679.2:g.7688425G>A	GRCh38
NC_000017.10:g.7591743G>A , CM000679.1:g.7591743G>A	GRCh37
NC_000017.9:g.7532468G>A	NCBI36
NG_017013.2:g.4126C>T , LRG_321:g.4126C>T
NG_028245.1:g.7355G>A , LRG_375:g.7355G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.-138G>A	ENSP00000513904.1:n.-138G>A
ENST00000316024.9:c.-224G>A	ENSP00000324203.5:n.-224G>A
ENST00000396463.6:c.-138G>A	ENSP00000379727.2:n.-138G>A
ENST00000431639.6:c.-1-223G>A	ENSP00000397219.2:n.-1-223G>A
ENST00000457584.6:c.-1-223G>A	ENSP00000411061.2:n.-1-223G>A
ENST00000498311.5:c.-138G>A	ENSP00000432991.1:n.-138G>A
NM_001143990.1:c.-1-223G>A	NP_001137462.1:n.-1-223G>A
NM_001143991.1:c.-1-223G>A	NP_001137463.1:n.-1-223G>A
NM_001143992.1:c.-138G>A	NP_001137464.1:n.-138G>A
NM_018081.2:c.-224G>A , LRG_375t1:c.-224G>A	NP_060551.2:n.-224G>A
XM_024450825.1:c.-138G>A	XP_024306593.1:n.-138G>A
XR_001752551.2:n.108G>A
NM_001143991.2:c.-1-223G>A	NP_001137463.1:n.-1-223G>A
NM_001143990.2:c.-1-223G>A	NP_001137462.1:n.-1-223G>A