Canonical Allele Identifier: CA2120139209

Gene: PROZ

Linked Data

• dbSNP Id: rs3024731

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113164394A>G , CM000675.2:g.113164394A>G	GRCh38
NC_000013.10:g.113818708A>G , CM000675.1:g.113818708A>G	GRCh37
NC_000013.9:g.112866709A>G	NCBI36
NG_031993.1:g.10741A>G
NG_031993.2:g.10741A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342783.5:c.440-119A>G	ENSP00000344458.4:n.440-119A>G
ENST00000375547.7:c.374-119A>G MANE Select	ENSP00000364697.2:n.374-119A>G
ENST00000342783.4:c.440-119A>G	ENSP00000344458.4:n.440-119A>G
ENST00000375547.6:c.374-119A>G	ENSP00000364697.2:n.374-119A>G
NM_001256134.1:c.440-119A>G	NP_001243063.1:n.440-119A>G
NM_003891.2:c.374-119A>G	NP_003882.1:n.374-119A>G
XM_011537525.1:c.584-119A>G	XP_011535827.1:n.584-119A>G
XM_017020812.1:c.575-119A>G	XP_016876301.1:n.575-119A>G
XM_017020813.1:c.440-119A>G	XP_016876302.1:n.440-119A>G
XR_001749707.1:n.561-119A>G
XR_001749708.1:n.561-119A>G
XR_001749709.1:n.561-119A>G
NM_003891.3:c.374-119A>G MANE Select	NP_003882.1:n.374-119A>G
NM_001256134.2:c.440-119A>G	NP_001243063.1:n.440-119A>G