Canonical Allele Identifier: CA7060869
Gene: PROZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113160968T>C , CM000675.2:g.113160968T>C GRCh38
NC_000013.10:g.113815282T>C , CM000675.1:g.113815282T>C GRCh37
NC_000013.9:g.112863283T>C NCBI36
NG_031993.1:g.7315T>C
NG_031993.2:g.7315T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000342783.5:c.321T>C ENSP00000344458.4:p.Tyr107=
ENST00000375547.7:c.255T>C MANE Select ENSP00000364697.2:p.Tyr85=
ENST00000342783.4:c.321T>C ENSP00000344458.4:p.Tyr107=
ENST00000375547.6:c.255T>C ENSP00000364697.2:p.Tyr85=
NM_001256134.1:c.321T>C NP_001243063.1:p.Tyr107=
NM_003891.2:c.255T>C NP_003882.1:p.Tyr85=
XM_011537525.1:c.465T>C XP_011535827.1:p.Tyr155=
XM_017020812.1:c.456T>C XP_016876301.1:p.Tyr152=
XM_017020813.1:c.321T>C XP_016876302.1:p.Tyr107=
XR_001749707.1:n.442T>C
XR_001749708.1:n.442T>C
XR_001749709.1:n.442T>C
NM_003891.3:c.255T>C MANE Select NP_003882.1:p.Tyr85=
NM_001256134.2:c.321T>C NP_001243063.1:p.Tyr107=