Canonical Allele Identifier: CA1202689104

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306706A= , CM000663.2:g.161306706A=	GRCh38
NC_000001.10:g.161276496A= , CM000663.1:g.161276496A=	GRCh37
NC_000001.9:g.159543120A=	NCBI36
NG_008055.1:g.8267T= , LRG_256:g.8267T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000526189.3:c.367+83T=	ENSP00000488104.2:n.367+83T=
ENST00000533357.5:c.448+2T= MANE Select	ENSP00000432943.1:n.448+2T=
ENST00000672287.2:c.-141+2T=	ENSP00000499818.2:n.-141+2T=
ENST00000672602.2:c.448+2T=	ENSP00000500814.2:n.448+2T=
ENST00000674861.1:n.511+2T=
ENST00000463290.5:c.448+2T=	ENSP00000431538.1:n.448+2T=
ENST00000491222.5:c.-141+2T=	ENSP00000431441.1:n.-141+2T=
ENST00000526189.2:c.111+83T=
ENST00000533357.4:c.448+2T=	ENSP00000432943.1:n.448+2T=
NM_000530.6:c.448+2T= , LRG_256t1:c.448+2T=	NP_000521.2:n.448+2T=
NM_000530.7:c.448+2T=	NP_000521.2:n.448+2T=
NM_001315491.1:c.448+2T=	NP_001302420.1:n.448+2T=
XM_017001321.2:c.478+2T=	XP_016856810.1:n.478+2T=
NM_000530.8:c.448+2T= MANE Select	NP_000521.2:n.448+2T=
NM_001315491.2:c.448+2T=	NP_001302420.1:n.448+2T=