Canonical Allele Identifier: CA2120155487

Gene: PROZ PCID2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113171786G= , CM000675.2:g.113171786G=	GRCh38
NC_000013.10:g.113826100G= , CM000675.1:g.113826100G=	GRCh37
NC_000013.9:g.112874101G=	NCBI36
NG_031993.1:g.18133G=
NG_031993.2:g.18133G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003891.3:c.884G= (PROZ) MANE Select	NP_003882.1:p.Arg295=
ENST00000375547.7:c.884G= (PROZ) MANE Select	ENSP00000364697.2:p.Arg295=
NM_001256134.1:c.950G= (PROZ)	NP_001243063.1:p.Arg317=
NM_001256134.2:c.950G= (PROZ)	NP_001243063.1:p.Arg317=
NM_003891.2:c.884G= (PROZ)	NP_003882.1:p.Arg295=
ENST00000342783.4:c.950G= (PROZ)	ENSP00000344458.4:p.Arg317=
ENST00000342783.5:c.950G= (PROZ)	ENSP00000344458.4:p.Arg317=
ENST00000375547.6:c.884G= (PROZ)	ENSP00000364697.2:p.Arg295=
XM_011537525.1:c.1094G= (PROZ)	XP_011535827.1:p.Arg365=
XM_017020812.1:c.1085G= (PROZ)	XP_016876301.1:p.Arg362=
XM_017020813.1:c.889+61G= (PROZ)	XP_016876302.1:n.889+61G=
XR_001749631.1:n.2237C= (PCID2)