Canonical Allele Identifier: CA2245953204

Gene: WRAP53

Linked Data

• dbSNP Id: rs1567569765

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7688440C>T , CM000679.2:g.7688440C>T	GRCh38
NC_000017.10:g.7591758C>T , CM000679.1:g.7591758C>T	GRCh37
NC_000017.9:g.7532483C>T	NCBI36
NG_017013.2:g.4111G>A , LRG_321:g.4111G>A
NG_028245.1:g.7370C>T , LRG_375:g.7370C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.-123C>T	ENSP00000513904.1:n.-123C>T
ENST00000698743.1:c.-123C>T	ENSP00000513905.1:n.-123C>T
ENST00000316024.9:c.-209C>T	ENSP00000324203.5:n.-209C>T
ENST00000396463.6:c.-123C>T	ENSP00000379727.2:n.-123C>T
ENST00000431639.6:c.-1-208C>T	ENSP00000397219.2:n.-1-208C>T
ENST00000457584.6:c.-1-208C>T	ENSP00000411061.2:n.-1-208C>T
ENST00000498311.5:c.-123C>T	ENSP00000432991.1:n.-123C>T
NM_001143990.1:c.-1-208C>T	NP_001137462.1:n.-1-208C>T
NM_001143991.1:c.-1-208C>T	NP_001137463.1:n.-1-208C>T
NM_001143992.1:c.-123C>T	NP_001137464.1:n.-123C>T
NM_018081.2:c.-209C>T , LRG_375t1:c.-209C>T	NP_060551.2:n.-209C>T
XM_024450825.1:c.-123C>T	XP_024306593.1:n.-123C>T
XR_001752551.2:n.123C>T
NM_001143991.2:c.-1-208C>T	NP_001137463.1:n.-1-208C>T
NM_001143990.2:c.-1-208C>T	NP_001137462.1:n.-1-208C>T