Canonical Allele Identifier: CA1202688190

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306104T= , CM000663.2:g.161306104T=	GRCh38
NC_000001.10:g.161275894T= , CM000663.1:g.161275894T=	GRCh37
NC_000001.9:g.159542518T=	NCBI36
NG_008055.1:g.8869A= , LRG_256:g.8869A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.564+4A=	ENSP00000488104.2:n.564+4A=
ENST00000533357.5:c.645+4A= MANE Select	ENSP00000432943.1:n.645+4A=
ENST00000672287.2:c.57+4A=	ENSP00000499818.2:n.57+4A=
ENST00000672602.2:c.645+4A=	ENSP00000500814.2:n.645+4A=
ENST00000674861.1:n.708+4A=
ENST00000463290.5:c.645+4A=	ENSP00000431538.1:n.645+4A=
ENST00000476410.1:n.109A=
ENST00000488271.1:n.83+4A=
ENST00000491222.5:c.57+4A=	ENSP00000431441.1:n.57+4A=
ENST00000526189.2:c.308+4A=
ENST00000533357.4:c.645+4A=	ENSP00000432943.1:n.645+4A=
NM_000530.6:c.645+4A= , LRG_256t1:c.645+4A=	NP_000521.2:n.645+4A=
NM_000530.7:c.645+4A=	NP_000521.2:n.645+4A=
NM_001315491.1:c.645+4A=	NP_001302420.1:n.645+4A=
XM_017001321.2:c.675+4A=	XP_016856810.1:n.675+4A=
NM_000530.8:c.645+4A= MANE Select	NP_000521.2:n.645+4A=
NM_001315491.2:c.645+4A=	NP_001302420.1:n.645+4A=