Canonical Allele Identifier: CA775172878

Gene: WRAP53

Linked Data

• dbSNP Id: rs1247050198
• gnomAD v3: 17-7688527-C-G
• gnomAD v4: 17-7688527-C-G
• MyVariant Identifiers: chr17:g.7591845C>G (hg19) ; chr17:g.7688527C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7688527C>G , CM000679.2:g.7688527C>G	GRCh38
NC_000017.10:g.7591845C>G , CM000679.1:g.7591845C>G	GRCh37
NC_000017.9:g.7532570C>G	NCBI36
NG_017013.2:g.4024G>C , LRG_321:g.4024G>C
NG_028245.1:g.7457C>G , LRG_375:g.7457C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.-36C>G	ENSP00000513904.1:n.-36C>G
ENST00000698743.1:c.-36C>G	ENSP00000513905.1:n.-36C>G
ENST00000698744.1:c.-36C>G	ENSP00000513906.1:n.-36C>G
ENST00000698745.1:c.-36C>G	ENSP00000513907.1:n.-36C>G
ENST00000698746.1:c.-36C>G	ENSP00000513908.1:n.-36C>G
ENST00000396463.7:c.-36C>G MANE Select	ENSP00000379727.3:n.-36C>G
ENST00000316024.9:c.-122C>G	ENSP00000324203.5:n.-122C>G
ENST00000396463.6:c.-36C>G	ENSP00000379727.2:n.-36C>G
ENST00000431639.6:c.-1-121C>G	ENSP00000397219.2:n.-1-121C>G
ENST00000457584.6:c.-1-121C>G	ENSP00000411061.2:n.-1-121C>G
ENST00000467699.5:n.51C>G
ENST00000498311.5:c.-36C>G	ENSP00000432991.1:n.-36C>G
ENST00000534050.5:c.-122C>G	ENSP00000434999.1:n.-122C>G
NM_001143990.1:c.-1-121C>G	NP_001137462.1:n.-1-121C>G
NM_001143991.1:c.-1-121C>G	NP_001137463.1:n.-1-121C>G
NM_001143992.1:c.-36C>G	NP_001137464.1:n.-36C>G
NM_018081.2:c.-122C>G , LRG_375t1:c.-122C>G	NP_060551.2:n.-122C>G
XM_024450824.1:c.-2111C>G	XP_024306592.1:n.-2111C>G
XM_024450825.1:c.-36C>G	XP_024306593.1:n.-36C>G
XR_001752551.2:n.210C>G
NM_001143991.2:c.-1-121C>G	NP_001137463.1:n.-1-121C>G
NM_001143992.2:c.-36C>G MANE Select	NP_001137464.1:n.-36C>G
NM_001143990.2:c.-1-121C>G	NP_001137462.1:n.-1-121C>G