Canonical Allele Identifier: CA7061088

Gene: PROZ PCID2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113171603G>A , CM000675.2:g.113171603G>A	GRCh38
NC_000013.10:g.113825917G>A , CM000675.1:g.113825917G>A	GRCh37
NC_000013.9:g.112873918G>A	NCBI36
NG_031993.1:g.17950G>A
NG_031993.2:g.17950G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342783.5:c.767G>A (PROZ)	ENSP00000344458.4:p.Arg256Lys
ENST00000375547.7:c.701G>A (PROZ) MANE Select	ENSP00000364697.2:p.Arg234Lys
ENST00000342783.4:c.767G>A (PROZ)	ENSP00000344458.4:p.Arg256Lys
ENST00000375547.6:c.701G>A (PROZ)	ENSP00000364697.2:p.Arg234Lys
NM_001256134.1:c.767G>A (PROZ)	NP_001243063.1:p.Arg256Lys
NM_003891.2:c.701G>A (PROZ)	NP_003882.1:p.Arg234Lys
XM_011537525.1:c.911G>A (PROZ)	XP_011535827.1:p.Arg304Lys
XM_017020812.1:c.902G>A (PROZ)	XP_016876301.1:p.Arg301Lys
XM_017020813.1:c.767G>A (PROZ)	XP_016876302.1:p.Arg256Lys
XR_001749631.1:n.2420C>T (PCID2)
NM_003891.3:c.701G>A (PROZ) MANE Select	NP_003882.1:p.Arg234Lys
NM_001256134.2:c.767G>A (PROZ)	NP_001243063.1:p.Arg256Lys