Canonical Allele Identifier: CA1202687661

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161305854C= , CM000663.2:g.161305854C=	GRCh38
NC_000001.10:g.161275644C= , CM000663.1:g.161275644C=	GRCh37
NC_000001.9:g.159542268C=	NCBI36
NG_008055.1:g.9119G= , LRG_256:g.9119G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.*22G=	ENSP00000488104.2:n.*22G=
ENST00000533357.5:c.*22G= MANE Select	ENSP00000432943.1:n.*22G=
ENST00000672287.2:c.*22G=	ENSP00000499818.2:n.*22G=
ENST00000672602.2:c.769G=	ENSP00000500814.2:p.Asp257=
ENST00000674861.1:n.832G=
ENST00000463290.5:c.*22G=	ENSP00000431538.1:n.*22G=
ENST00000476410.1:n.359G=
ENST00000488271.1:n.207G=
ENST00000491222.5:c.*22G=	ENSP00000431441.1:n.*22G=
ENST00000526189.2:c.432G=
ENST00000533357.4:c.*22G=	ENSP00000432943.1:n.*22G=
NM_000530.6:c.*22G= , LRG_256t1:c.*22G=	NP_000521.2:n.*22G=
NM_000530.7:c.*22G=	NP_000521.2:n.*22G=
NM_001315491.1:c.769G=	NP_001302420.1:p.Asp257=
XM_017001321.2:c.675+254G=	XP_016856810.1:n.675+254G=
NM_000530.8:c.*22G= MANE Select	NP_000521.2:n.*22G=
NM_001315491.2:c.769G=	NP_001302420.1:p.Asp257=