Canonical Allele Identifier: CA13824990
Gene: PROZ HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113159539A>G , CM000675.2:g.113159539A>G GRCh38
NC_000013.10:g.113813853A>G , CM000675.1:g.113813853A>G GRCh37
NC_000013.9:g.112861854A>G NCBI36
NG_031993.1:g.5886A>G
NG_031993.2:g.5886A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342783.5:c.136+275A>G ENSP00000344458.4:n.136+275A>G
ENST00000375547.7:c.71-475A>G MANE Select ENSP00000364697.2:n.71-475A>G
ENST00000342783.4:c.136+275A>G ENSP00000344458.4:n.136+275A>G
ENST00000375547.6:c.71-475A>G ENSP00000364697.2:n.71-475A>G
NM_001256134.1:c.136+275A>G NP_001243063.1:n.136+275A>G
NM_003891.2:c.71-475A>G NP_003882.1:n.71-475A>G
XM_011537525.1:c.280+275A>G XP_011535827.1:n.280+275A>G
XM_017020812.1:c.271+275A>G XP_016876301.1:n.271+275A>G
XM_017020813.1:c.136+275A>G XP_016876302.1:n.136+275A>G
XR_001749707.1:n.257+275A>G
XR_001749708.1:n.257+275A>G
XR_001749709.1:n.257+275A>G
NM_003891.3:c.71-475A>G MANE Select NP_003882.1:n.71-475A>G
NM_001256134.2:c.136+275A>G NP_001243063.1:n.136+275A>G
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