Canonical Allele Identifier: CA2120132887

Gene: PROZ

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113160151G= , CM000675.2:g.113160151G=	GRCh38
NC_000013.10:g.113814465G= , CM000675.1:g.113814465G=	GRCh37
NC_000013.9:g.112862466G=	NCBI36
NG_031993.1:g.6498G=
NG_031993.2:g.6498G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003891.3:c.208G= MANE Select	NP_003882.1:p.Glu70=
ENST00000375547.7:c.208G= MANE Select	ENSP00000364697.2:p.Glu70=
NM_001256134.1:c.274G=	NP_001243063.1:p.Glu92=
NM_001256134.2:c.274G=	NP_001243063.1:p.Glu92=
NM_003891.2:c.208G=	NP_003882.1:p.Glu70=
ENST00000342783.4:c.274G=	ENSP00000344458.4:p.Glu92=
ENST00000342783.5:c.274G=	ENSP00000344458.4:p.Glu92=
ENST00000375547.6:c.208G=	ENSP00000364697.2:p.Glu70=
XM_011537525.1:c.418G=	XP_011535827.1:p.Glu140=
XM_017020812.1:c.409G=	XP_016876301.1:p.Glu137=
XM_017020813.1:c.274G=	XP_016876302.1:p.Glu92=
XR_001749707.1:n.395G=
XR_001749708.1:n.395G=
XR_001749709.1:n.395G=