Canonical Allele Identifier: CA497926578

Gene: WRAP53

Linked Data

• gnomAD v4: 17-7689011-A-G
• MyVariant Identifiers: chr17:g.7592329A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7689011A>G , CM000679.2:g.7689011A>G	GRCh38
NC_000017.10:g.7592329A>G , CM000679.1:g.7592329A>G	GRCh37
NC_000017.9:g.7533054A>G	NCBI36
NG_017013.2:g.3540T>C , LRG_321:g.3540T>C
NG_028245.1:g.7941A>G , LRG_375:g.7941A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.363A>G	ENSP00000513904.1:p.Pro121=
ENST00000698743.1:c.363A>G	ENSP00000513905.1:p.Pro121=
ENST00000698744.1:c.363A>G	ENSP00000513906.1:p.Pro121=
ENST00000698745.1:c.363A>G	ENSP00000513907.1:p.Pro121=
ENST00000698746.1:c.363A>G	ENSP00000513908.1:p.Pro121=
ENST00000396463.7:c.363A>G MANE Select	ENSP00000379727.3:p.Pro121=
ENST00000316024.9:c.363A>G	ENSP00000324203.5:p.Pro121=
ENST00000396463.6:c.363A>G	ENSP00000379727.2:p.Pro121=
ENST00000431639.6:c.363A>G	ENSP00000397219.2:p.Pro121=
ENST00000457584.6:c.363A>G	ENSP00000411061.2:p.Pro121=
ENST00000467699.5:n.449A>G
ENST00000498311.5:c.363A>G	ENSP00000432991.1:p.Pro121=
ENST00000534050.5:c.363A>G	ENSP00000434999.1:p.Pro121=
NM_001143990.1:c.363A>G	NP_001137462.1:p.Pro121=
NM_001143991.1:c.363A>G	NP_001137463.1:p.Pro121=
NM_001143992.1:c.363A>G	NP_001137464.1:p.Pro121=
NM_018081.2:c.363A>G , LRG_375t1:c.363A>G	NP_060551.2:p.Pro121=
XM_011523952.2:c.-270A>G	XP_011522254.1:n.-270A>G
XM_024450824.1:c.-1713A>G	XP_024306592.1:n.-1713A>G
XM_024450825.1:c.363A>G	XP_024306593.1:p.Pro121=
XR_001752551.2:n.608A>G
NM_001143991.2:c.363A>G	NP_001137463.1:p.Pro121=
NM_001143992.2:c.363A>G MANE Select	NP_001137464.1:p.Pro121=
NM_001143990.2:c.363A>G	NP_001137462.1:p.Pro121=