Canonical Allele Identifier: CA1141581155
Gene: MPZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161306763G= , CM000663.2:g.161306763G= GRCh38
NC_000001.10:g.161276553G= , CM000663.1:g.161276553G= GRCh37
NC_000001.9:g.159543177G= NCBI36
NG_008055.1:g.8210C= , LRG_256:g.8210C=

Transcript Alleles

HGVS Amino-acid change
ENST00000526189.3:c.367+26C= ENSP00000488104.2:n.367+26C=
ENST00000533357.5:c.393C= MANE Select ENSP00000432943.1:p.Asn131=
ENST00000672287.2:c.-196C= ENSP00000499818.2:n.-196C=
ENST00000672602.2:c.393C= ENSP00000500814.2:p.Asn131=
ENST00000674861.1:n.456C=
ENST00000463290.5:c.393C= ENSP00000431538.1:p.Asn131=
ENST00000491222.5:c.-196C= ENSP00000431441.1:n.-196C=
ENST00000526189.2:c.111+26C=
ENST00000533357.4:c.393C= ENSP00000432943.1:p.Asn131=
NM_000530.6:c.393C= , LRG_256t1:c.393C= NP_000521.2:p.Asn131=
NM_000530.7:c.393C= NP_000521.2:p.Asn131=
NM_001315491.1:c.393C= NP_001302420.1:p.Asn131=
XM_017001321.2:c.423C= XP_016856810.1:p.Asn141=
NM_000530.8:c.393C= MANE Select NP_000521.2:p.Asn131=
NM_001315491.2:c.393C= NP_001302420.1:p.Asn131=