Canonical Allele Identifier: CA2579753988
Gene: MPZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161306108del , CM000663.2:g.161306108del GRCh38
NC_000001.10:g.161275898del , CM000663.1:g.161275898del GRCh37
NC_000001.9:g.159542522del NCBI36
NG_008055.1:g.8866del , LRG_256:g.8866del

Transcript Alleles

HGVS Amino-acid Change
ENST00000526189.3:c.564+1del
ENST00000533357.5:c.645+1del
ENST00000672287.2:c.57+1del
ENST00000672602.2:c.645+1del
ENST00000674861.1:n.708+1del
ENST00000463290.5:c.645+1del
ENST00000476410.1:n.106del
ENST00000488271.1:n.83+1del
ENST00000491222.5:c.57+1del
ENST00000526189.2:c.308+1del
ENST00000533357.4:c.645+1del
NM_000530.6:c.645+1del , LRG_256t1:c.645+1del
NM_000530.7:c.645+1del
NM_001315491.1:c.645+1del
XM_017001321.2:c.675+1del
NM_000530.8:c.645+1del
NM_001315491.2:c.645+1del