Canonical Allele Identifier: CA7061089

Gene: PROZ PCID2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113171606C>T , CM000675.2:g.113171606C>T	GRCh38
NC_000013.10:g.113825920C>T , CM000675.1:g.113825920C>T	GRCh37
NC_000013.9:g.112873921C>T	NCBI36
NG_031993.1:g.17953C>T
NG_031993.2:g.17953C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342783.5:c.770C>T (PROZ)	ENSP00000344458.4:p.Thr257Met
ENST00000375547.7:c.704C>T (PROZ) MANE Select	ENSP00000364697.2:p.Thr235Met
ENST00000342783.4:c.770C>T (PROZ)	ENSP00000344458.4:p.Thr257Met
ENST00000375547.6:c.704C>T (PROZ)	ENSP00000364697.2:p.Thr235Met
NM_001256134.1:c.770C>T (PROZ)	NP_001243063.1:p.Thr257Met
NM_003891.2:c.704C>T (PROZ)	NP_003882.1:p.Thr235Met
XM_011537525.1:c.914C>T (PROZ)	XP_011535827.1:p.Thr305Met
XM_017020812.1:c.905C>T (PROZ)	XP_016876301.1:p.Thr302Met
XM_017020813.1:c.770C>T (PROZ)	XP_016876302.1:p.Thr257Met
XR_001749631.1:n.2417G>A (PCID2)
NM_003891.3:c.704C>T (PROZ) MANE Select	NP_003882.1:p.Thr235Met
NM_001256134.2:c.770C>T (PROZ)	NP_001243063.1:p.Thr257Met