Canonical Allele Identifier: CA2245954204

Gene: WRAP53

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7689033A= , CM000679.2:g.7689033A=	GRCh38
NC_000017.10:g.7592351A= , CM000679.1:g.7592351A=	GRCh37
NC_000017.9:g.7533076A=	NCBI36
NG_017013.2:g.3518T= , LRG_321:g.3518T=
NG_028245.1:g.7963A= , LRG_375:g.7963A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.385A=	ENSP00000513904.1:p.Met129=
ENST00000698743.1:c.385A=	ENSP00000513905.1:p.Met129=
ENST00000698744.1:c.385A=	ENSP00000513906.1:p.Met129=
ENST00000698745.1:c.385A=	ENSP00000513907.1:p.Met129=
ENST00000698746.1:c.385A=	ENSP00000513908.1:p.Met129=
ENST00000396463.7:c.385A= MANE Select	ENSP00000379727.3:p.Met129=
ENST00000316024.9:c.385A=	ENSP00000324203.5:p.Met129=
ENST00000396463.6:c.385A=	ENSP00000379727.2:p.Met129=
ENST00000431639.6:c.385A=	ENSP00000397219.2:p.Met129=
ENST00000457584.6:c.385A=	ENSP00000411061.2:p.Met129=
ENST00000467699.5:n.471A=
ENST00000498311.5:c.385A=	ENSP00000432991.1:p.Met129=
ENST00000534050.5:c.385A=	ENSP00000434999.1:p.Met129=
NM_001143990.1:c.385A=	NP_001137462.1:p.Met129=
NM_001143991.1:c.385A=	NP_001137463.1:p.Met129=
NM_001143992.1:c.385A=	NP_001137464.1:p.Met129=
NM_018081.2:c.385A= , LRG_375t1:c.385A=	NP_060551.2:p.Met129=
XM_011523952.2:c.-248A=	XP_011522254.1:n.-248A=
XM_024450824.1:c.-1691A=	XP_024306592.1:n.-1691A=
XM_024450825.1:c.385A=	XP_024306593.1:p.Met129=
XR_001752551.2:n.630A=
NM_001143991.2:c.385A=	NP_001137463.1:p.Met129=
NM_001143992.2:c.385A= MANE Select	NP_001137464.1:p.Met129=
NM_001143990.2:c.385A=	NP_001137462.1:p.Met129=