Canonical Allele Identifier: CA343349564
Gene: MPZ HGNC NCBI

Linked Data

ClinVar Variation Id: 531678
dbSNP Id: rs1553259683

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161306858G>A , CM000663.2:g.161306858G>A GRCh38
NC_000001.10:g.161276648G>A , CM000663.1:g.161276648G>A GRCh37
NC_000001.9:g.159543272G>A NCBI36
NG_008055.1:g.8115C>T , LRG_256:g.8115C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000526189.3:c.298C>T ENSP00000488104.2:p.Gln100Ter
ENST00000533357.5:c.298C>T MANE Select ENSP00000432943.1:p.Gln100Ter
ENST00000672287.2:c.-291C>T ENSP00000499818.2:n.-291C>T
ENST00000672602.2:c.298C>T ENSP00000500814.2:p.Gln100Ter
ENST00000674861.1:n.361C>T
ENST00000463290.5:c.298C>T ENSP00000431538.1:p.Gln100Ter
ENST00000491222.5:c.-291C>T ENSP00000431441.1:n.-291C>T
ENST00000526189.2:c.42C>T
ENST00000533357.4:c.298C>T ENSP00000432943.1:p.Gln100Ter
NM_000530.6:c.298C>T , LRG_256t1:c.298C>T NP_000521.2:p.Gln100Ter
NM_000530.7:c.298C>T NP_000521.2:p.Gln100Ter
NM_001315491.1:c.298C>T NP_001302420.1:p.Gln100Ter
XM_017001321.2:c.328C>T XP_016856810.1:p.Gln110Ter
NM_000530.8:c.298C>T MANE Select NP_000521.2:p.Gln100Ter
NM_001315491.2:c.298C>T NP_001302420.1:p.Gln100Ter