Canonical Allele Identifier: CA1202688048

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306002T= , CM000663.2:g.161306002T=	GRCh38
NC_000001.10:g.161275792T= , CM000663.1:g.161275792T=	GRCh37
NC_000001.9:g.159542416T=	NCBI36
NG_008055.1:g.8971A= , LRG_256:g.8971A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.565-25A=	ENSP00000488104.2:n.565-25A=
ENST00000533357.5:c.646-25A= MANE Select	ENSP00000432943.1:n.646-25A=
ENST00000672287.2:c.58-25A=	ENSP00000499818.2:n.58-25A=
ENST00000672602.2:c.646-25A=	ENSP00000500814.2:n.646-25A=
ENST00000674861.1:n.709-25A=
ENST00000463290.5:c.646-25A=	ENSP00000431538.1:n.646-25A=
ENST00000476410.1:n.211A=
ENST00000488271.1:n.84-25A=
ENST00000491222.5:c.58-25A=	ENSP00000431441.1:n.58-25A=
ENST00000526189.2:c.309-25A=
ENST00000533357.4:c.646-25A=	ENSP00000432943.1:n.646-25A=
NM_000530.6:c.646-25A= , LRG_256t1:c.646-25A=	NP_000521.2:n.646-25A=
NM_000530.7:c.646-25A=	NP_000521.2:n.646-25A=
NM_001315491.1:c.646-25A=	NP_001302420.1:n.646-25A=
XM_017001321.2:c.675+106A=	XP_016856810.1:n.675+106A=
NM_000530.8:c.646-25A= MANE Select	NP_000521.2:n.646-25A=
NM_001315491.2:c.646-25A=	NP_001302420.1:n.646-25A=