Canonical Allele Identifier: CA1143461543

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161305982G= , CM000663.2:g.161305982G=	GRCh38
NC_000001.10:g.161275772G= , CM000663.1:g.161275772G=	GRCh37
NC_000001.9:g.159542396G=	NCBI36
NG_008055.1:g.8991C= , LRG_256:g.8991C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.565-5C=	ENSP00000488104.2:n.565-5C=
ENST00000533357.5:c.646-5C= MANE Select	ENSP00000432943.1:n.646-5C=
ENST00000672287.2:c.58-5C=	ENSP00000499818.2:n.58-5C=
ENST00000672602.2:c.646-5C=	ENSP00000500814.2:n.646-5C=
ENST00000674861.1:n.709-5C=
ENST00000463290.5:c.646-5C=	ENSP00000431538.1:n.646-5C=
ENST00000476410.1:n.231C=
ENST00000488271.1:n.84-5C=
ENST00000491222.5:c.58-5C=	ENSP00000431441.1:n.58-5C=
ENST00000526189.2:c.309-5C=
ENST00000533357.4:c.646-5C=	ENSP00000432943.1:n.646-5C=
NM_000530.6:c.646-5C= , LRG_256t1:c.646-5C=	NP_000521.2:n.646-5C=
NM_000530.7:c.646-5C=	NP_000521.2:n.646-5C=
NM_001315491.1:c.646-5C=	NP_001302420.1:n.646-5C=
XM_017001321.2:c.675+126C=	XP_016856810.1:n.675+126C=
NM_000530.8:c.646-5C= MANE Select	NP_000521.2:n.646-5C=
NM_001315491.2:c.646-5C=	NP_001302420.1:n.646-5C=