Canonical Allele Identifier: CA343343783
Gene: MPZ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161305885A>T , CM000663.2:g.161305885A>T GRCh38
NC_000001.10:g.161275675A>T , CM000663.1:g.161275675A>T GRCh37
NC_000001.9:g.159542299A>T NCBI36
NG_008055.1:g.9088T>A , LRG_256:g.9088T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000526189.3:c.657T>A ENSP00000488104.2:p.Asp219Glu
ENST00000533357.5:c.738T>A MANE Select ENSP00000432943.1:p.Asp246Glu
ENST00000672287.2:c.150T>A ENSP00000499818.2:p.Asp50Glu
ENST00000672602.2:c.738T>A ENSP00000500814.2:p.Asp246Glu
ENST00000674861.1:n.801T>A
ENST00000463290.5:c.738T>A ENSP00000431538.1:p.Asp246Glu
ENST00000476410.1:n.328T>A
ENST00000488271.1:n.176T>A
ENST00000491222.5:c.150T>A ENSP00000431441.1:p.Asp50Glu
ENST00000526189.2:c.401T>A
ENST00000533357.4:c.738T>A ENSP00000432943.1:p.Asp246Glu
NM_000530.6:c.738T>A , LRG_256t1:c.738T>A NP_000521.2:p.Asp246Glu
NM_000530.7:c.738T>A NP_000521.2:p.Asp246Glu
NM_001315491.1:c.738T>A NP_001302420.1:p.Asp246Glu
XM_017001321.2:c.675+223T>A XP_016856810.1:n.675+223T>A
NM_000530.8:c.738T>A MANE Select NP_000521.2:p.Asp246Glu
NM_001315491.2:c.738T>A NP_001302420.1:p.Asp246Glu