Canonical Allele Identifier: CA397854596

Gene: WRAP53

Linked Data

• MyVariant Identifiers: chr17:g.7591974C>G (hg19) ; chr17:g.7688656C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7688656C>G , CM000679.2:g.7688656C>G	GRCh38
NC_000017.10:g.7591974C>G , CM000679.1:g.7591974C>G	GRCh37
NC_000017.9:g.7532699C>G	NCBI36
NG_017013.2:g.3895G>C , LRG_321:g.3895G>C
NG_028245.1:g.7586C>G , LRG_375:g.7586C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.8C>G	ENSP00000513904.1:p.Thr3Ser
ENST00000698743.1:c.8C>G	ENSP00000513905.1:p.Thr3Ser
ENST00000698744.1:c.8C>G	ENSP00000513906.1:p.Thr3Ser
ENST00000698745.1:c.8C>G	ENSP00000513907.1:p.Thr3Ser
ENST00000698746.1:c.8C>G	ENSP00000513908.1:p.Thr3Ser
ENST00000396463.7:c.8C>G MANE Select	ENSP00000379727.3:p.Thr3Ser
ENST00000316024.9:c.8C>G	ENSP00000324203.5:p.Thr3Ser
ENST00000396463.6:c.8C>G	ENSP00000379727.2:p.Thr3Ser
ENST00000431639.6:c.8C>G	ENSP00000397219.2:p.Thr3Ser
ENST00000457584.6:c.8C>G	ENSP00000411061.2:p.Thr3Ser
ENST00000467699.5:n.94C>G
ENST00000498311.5:c.8C>G	ENSP00000432991.1:p.Thr3Ser
ENST00000534050.5:c.8C>G	ENSP00000434999.1:p.Thr3Ser
NM_001143990.1:c.8C>G	NP_001137462.1:p.Thr3Ser
NM_001143991.1:c.8C>G	NP_001137463.1:p.Thr3Ser
NM_001143992.1:c.8C>G	NP_001137464.1:p.Thr3Ser
NM_018081.2:c.8C>G , LRG_375t1:c.8C>G	NP_060551.2:p.Thr3Ser
XM_024450824.1:c.-2068C>G	XP_024306592.1:n.-2068C>G
XM_024450825.1:c.8C>G	XP_024306593.1:p.Thr3Ser
XR_001752551.2:n.253C>G
NM_001143991.2:c.8C>G	NP_001137463.1:p.Thr3Ser
NM_001143992.2:c.8C>G MANE Select	NP_001137464.1:p.Thr3Ser
NM_001143990.2:c.8C>G	NP_001137462.1:p.Thr3Ser