Canonical Allele Identifier: CA13824994

Gene: PROZ

Linked Data

• dbSNP Id: rs3024731
• gnomAD v2: 13-113818708-A-T
• gnomAD v3: 13-113164394-A-T
• gnomAD v4: 13-113164394-A-T
• MyVariant Identifiers: chr13:g.113818708A>T (hg19) ; chr13:g.113164394A>T (hg38)

Genomic Alleles

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

Transcript Alleles

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