Canonical Allele Identifier: CA1202688140

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306067G= , CM000663.2:g.161306067G=	GRCh38
NC_000001.10:g.161275857G= , CM000663.1:g.161275857G=	GRCh37
NC_000001.9:g.159542481G=	NCBI36
NG_008055.1:g.8906C= , LRG_256:g.8906C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.564+41C=	ENSP00000488104.2:n.564+41C=
ENST00000533357.5:c.645+41C= MANE Select	ENSP00000432943.1:n.645+41C=
ENST00000672287.2:c.57+41C=	ENSP00000499818.2:n.57+41C=
ENST00000672602.2:c.645+41C=	ENSP00000500814.2:n.645+41C=
ENST00000674861.1:n.708+41C=
ENST00000463290.5:c.645+41C=	ENSP00000431538.1:n.645+41C=
ENST00000476410.1:n.146C=
ENST00000488271.1:n.83+41C=
ENST00000491222.5:c.57+41C=	ENSP00000431441.1:n.57+41C=
ENST00000526189.2:c.308+41C=
ENST00000533357.4:c.645+41C=	ENSP00000432943.1:n.645+41C=
NM_000530.6:c.645+41C= , LRG_256t1:c.645+41C=	NP_000521.2:n.645+41C=
NM_000530.7:c.645+41C=	NP_000521.2:n.645+41C=
NM_001315491.1:c.645+41C=	NP_001302420.1:n.645+41C=
XM_017001321.2:c.675+41C=	XP_016856810.1:n.675+41C=
NM_000530.8:c.645+41C= MANE Select	NP_000521.2:n.645+41C=
NM_001315491.2:c.645+41C=	NP_001302420.1:n.645+41C=