Canonical Allele Identifier: CA497731425

Gene: WRAP53

Linked Data

• gnomAD v4: 17-7689062-A-C
• MyVariant Identifiers: chr17:g.7592380A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7689062A>C , CM000679.2:g.7689062A>C	GRCh38
NC_000017.10:g.7592380A>C , CM000679.1:g.7592380A>C	GRCh37
NC_000017.9:g.7533105A>C	NCBI36
NG_017013.2:g.3489T>G , LRG_321:g.3489T>G
NG_028245.1:g.7992A>C , LRG_375:g.7992A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.414A>C	ENSP00000513904.1:p.Ala138=
ENST00000698743.1:c.414A>C	ENSP00000513905.1:p.Ala138=
ENST00000698744.1:c.414A>C	ENSP00000513906.1:p.Ala138=
ENST00000698745.1:c.414A>C	ENSP00000513907.1:p.Ala138=
ENST00000698746.1:c.414A>C	ENSP00000513908.1:p.Ala138=
ENST00000396463.7:c.414A>C MANE Select	ENSP00000379727.3:p.Ala138=
ENST00000316024.9:c.414A>C	ENSP00000324203.5:p.Ala138=
ENST00000396463.6:c.414A>C	ENSP00000379727.2:p.Ala138=
ENST00000431639.6:c.414A>C	ENSP00000397219.2:p.Ala138=
ENST00000457584.6:c.414A>C	ENSP00000411061.2:p.Ala138=
ENST00000467699.5:n.500A>C
ENST00000498311.5:c.414A>C	ENSP00000432991.1:p.Ala138=
ENST00000534050.5:c.414A>C	ENSP00000434999.1:p.Ala138=
NM_001143990.1:c.414A>C	NP_001137462.1:p.Ala138=
NM_001143991.1:c.414A>C	NP_001137463.1:p.Ala138=
NM_001143992.1:c.414A>C	NP_001137464.1:p.Ala138=
NM_018081.2:c.414A>C , LRG_375t1:c.414A>C	NP_060551.2:p.Ala138=
XM_011523952.2:c.-219A>C	XP_011522254.1:n.-219A>C
XM_024450824.1:c.-1662A>C	XP_024306592.1:n.-1662A>C
XM_024450825.1:c.414A>C	XP_024306593.1:p.Ala138=
XR_001752551.2:n.659A>C
NM_001143991.2:c.414A>C	NP_001137463.1:p.Ala138=
NM_001143992.2:c.414A>C MANE Select	NP_001137464.1:p.Ala138=
NM_001143990.2:c.414A>C	NP_001137462.1:p.Ala138=