Canonical Allele Identifier: CA2245953182

Gene: WRAP53

Linked Data

• dbSNP Id: rs1270954199

Genomic Alleles

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

Transcript Alleles

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