Canonical Allele Identifier: CA624729490
Gene: WRAP53 HGNC NCBI

Linked Data

dbSNP Id: rs1270954199
gnomAD v2: 17-7591729-T-A
gnomAD v3: 17-7688411-T-A
gnomAD v4: 17-7688411-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7688411T>A , CM000679.2:g.7688411T>A GRCh38
NC_000017.10:g.7591729T>A , CM000679.1:g.7591729T>A GRCh37
NC_000017.9:g.7532454T>A NCBI36
NG_017013.2:g.4140A>T , LRG_321:g.4140A>T
NG_028245.1:g.7341T>A , LRG_375:g.7341T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698742.1:c.-152T>A ENSP00000513904.1:n.-152T>A
ENST00000316024.9:c.-238T>A ENSP00000324203.5:n.-238T>A
ENST00000396463.6:c.-152T>A ENSP00000379727.2:n.-152T>A
ENST00000431639.6:c.-1-237T>A ENSP00000397219.2:n.-1-237T>A
ENST00000457584.6:c.-1-237T>A ENSP00000411061.2:n.-1-237T>A
ENST00000498311.5:c.-152T>A ENSP00000432991.1:n.-152T>A
NM_001143990.1:c.-1-237T>A NP_001137462.1:n.-1-237T>A
NM_001143991.1:c.-1-237T>A NP_001137463.1:n.-1-237T>A
NM_001143992.1:c.-152T>A NP_001137464.1:n.-152T>A
NM_018081.2:c.-238T>A , LRG_375t1:c.-238T>A NP_060551.2:n.-238T>A
XM_024450825.1:c.-152T>A XP_024306593.1:n.-152T>A
XR_001752551.2:n.94T>A
NM_001143991.2:c.-1-237T>A NP_001137463.1:n.-1-237T>A
NM_001143990.2:c.-1-237T>A NP_001137462.1:n.-1-237T>A