Canonical Allele Identifier: CA1202689584
Gene: MPZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161306821A= , CM000663.2:g.161306821A= GRCh38
NC_000001.10:g.161276611A= , CM000663.1:g.161276611A= GRCh37
NC_000001.9:g.159543235A= NCBI36
NG_008055.1:g.8152T= , LRG_256:g.8152T=

Transcript Alleles

HGVS Amino-acid change
ENST00000526189.3:c.335T= ENSP00000488104.2:p.Ile112=
ENST00000533357.5:c.335T= MANE Select ENSP00000432943.1:p.Ile112=
ENST00000672287.2:c.-254T= ENSP00000499818.2:n.-254T=
ENST00000672602.2:c.335T= ENSP00000500814.2:p.Ile112=
ENST00000674861.1:n.398T=
ENST00000463290.5:c.335T= ENSP00000431538.1:p.Ile112=
ENST00000491222.5:c.-254T= ENSP00000431441.1:n.-254T=
ENST00000526189.2:c.79T=
ENST00000533357.4:c.335T= ENSP00000432943.1:p.Ile112=
NM_000530.6:c.335T= , LRG_256t1:c.335T= NP_000521.2:p.Ile112=
NM_000530.7:c.335T= NP_000521.2:p.Ile112=
NM_001315491.1:c.335T= NP_001302420.1:p.Ile112=
XM_017001321.2:c.365T= XP_016856810.1:p.Ile122=
NM_000530.8:c.335T= MANE Select NP_000521.2:p.Ile112=
NM_001315491.2:c.335T= NP_001302420.1:p.Ile112=