Canonical Allele Identifier: CA343348596
Gene: MPZ HGNC NCBI

Linked Data

ClinVar Variation Id: 963646
ClinVar RCV Id: RCV001237700
dbSNP Id: rs1571818744

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161306749A>C , CM000663.2:g.161306749A>C GRCh38
NC_000001.10:g.161276539A>C , CM000663.1:g.161276539A>C GRCh37
NC_000001.9:g.159543163A>C NCBI36
NG_008055.1:g.8224T>G , LRG_256:g.8224T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000526189.3:c.367+40T>G ENSP00000488104.2:n.367+40T>G
ENST00000533357.5:c.407T>G MANE Select ENSP00000432943.1:p.Val136Gly
ENST00000672287.2:c.-182T>G ENSP00000499818.2:n.-182T>G
ENST00000672602.2:c.407T>G ENSP00000500814.2:p.Val136Gly
ENST00000674861.1:n.470T>G
ENST00000463290.5:c.407T>G ENSP00000431538.1:p.Val136Gly
ENST00000491222.5:c.-182T>G ENSP00000431441.1:n.-182T>G
ENST00000526189.2:c.111+40T>G
ENST00000533357.4:c.407T>G ENSP00000432943.1:p.Val136Gly
NM_000530.6:c.407T>G , LRG_256t1:c.407T>G NP_000521.2:p.Val136Gly
NM_000530.7:c.407T>G NP_000521.2:p.Val136Gly
NM_001315491.1:c.407T>G NP_001302420.1:p.Val136Gly
XM_017001321.2:c.437T>G XP_016856810.1:p.Val146Gly
NM_000530.8:c.407T>G MANE Select NP_000521.2:p.Val136Gly
NM_001315491.2:c.407T>G NP_001302420.1:p.Val136Gly