Canonical Allele Identifier: CA1141581156
Gene: MPZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161307268T= , CM000663.2:g.161307268T= GRCh38
NC_000001.10:g.161277058T= , CM000663.1:g.161277058T= GRCh37
NC_000001.9:g.159543682T= NCBI36
NG_008055.1:g.7705A= , LRG_256:g.7705A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000526189.3:c.224A= ENSP00000488104.2:p.Asp75=
ENST00000533357.5:c.224A= MANE Select ENSP00000432943.1:p.Asp75=
ENST00000672287.2:c.-365A= ENSP00000499818.2:n.-365A=
ENST00000672602.2:c.224A= ENSP00000500814.2:p.Asp75=
ENST00000674861.1:n.287A=
ENST00000463290.5:c.224A= ENSP00000431538.1:p.Asp75=
ENST00000491222.5:c.-365A= ENSP00000431441.1:n.-365A=
ENST00000533357.4:c.224A= ENSP00000432943.1:p.Asp75=
NM_000530.6:c.224A= , LRG_256t1:c.224A= NP_000521.2:p.Asp75=
NM_000530.7:c.224A= NP_000521.2:p.Asp75=
NM_001315491.1:c.224A= NP_001302420.1:p.Asp75=
XM_017001321.2:c.254A= XP_016856810.1:p.Asp85=
NM_000530.8:c.224A= MANE Select NP_000521.2:p.Asp75=
NM_001315491.2:c.224A= NP_001302420.1:p.Asp75=