Canonical Allele Identifier: CA1202689144
Gene: MPZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161306721A= , CM000663.2:g.161306721A= GRCh38
NC_000001.10:g.161276511A= , CM000663.1:g.161276511A= GRCh37
NC_000001.9:g.159543135A= NCBI36
NG_008055.1:g.8252T= , LRG_256:g.8252T=

Transcript Alleles

HGVS Amino-acid change
ENST00000526189.3:c.367+68T= ENSP00000488104.2:n.367+68T=
ENST00000533357.5:c.435T= MANE Select ENSP00000432943.1:p.Tyr145=
ENST00000672287.2:c.-154T= ENSP00000499818.2:n.-154T=
ENST00000672602.2:c.435T= ENSP00000500814.2:p.Tyr145=
ENST00000674861.1:n.498T=
ENST00000463290.5:c.435T= ENSP00000431538.1:p.Tyr145=
ENST00000491222.5:c.-154T= ENSP00000431441.1:n.-154T=
ENST00000526189.2:c.111+68T=
ENST00000533357.4:c.435T= ENSP00000432943.1:p.Tyr145=
NM_000530.6:c.435T= , LRG_256t1:c.435T= NP_000521.2:p.Tyr145=
NM_000530.7:c.435T= NP_000521.2:p.Tyr145=
NM_001315491.1:c.435T= NP_001302420.1:p.Tyr145=
XM_017001321.2:c.465T= XP_016856810.1:p.Tyr155=
NM_000530.8:c.435T= MANE Select NP_000521.2:p.Tyr145=
NM_001315491.2:c.435T= NP_001302420.1:p.Tyr145=