Canonical Allele Identifier: CA1202693386

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161309880C= , CM000663.2:g.161309880C=	GRCh38
NC_000001.10:g.161279670C= , CM000663.1:g.161279670C=	GRCh37
NC_000001.9:g.159546294C=	NCBI36
NG_008055.1:g.5093G= , LRG_256:g.5093G=
NG_012767.1:g.505C= , LRG_317:g.505C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.26G=	ENSP00000488104.2:p.Ser9=
ENST00000533357.5:c.26G= MANE Select	ENSP00000432943.1:p.Ser9=
ENST00000672602.2:c.26G=	ENSP00000500814.2:p.Ser9=
ENST00000674861.1:n.89G=
ENST00000463290.5:c.26G=	ENSP00000431538.1:p.Ser9=
ENST00000533357.4:c.26G=	ENSP00000432943.1:p.Ser9=
NM_000530.6:c.26G= , LRG_256t1:c.26G=	NP_000521.2:p.Ser9=
NM_000530.7:c.26G=	NP_000521.2:p.Ser9=
NM_001315491.1:c.26G=	NP_001302420.1:p.Ser9=
XM_017001321.2:c.56G=	XP_016856810.1:p.Ser19=
NM_000530.8:c.26G= MANE Select	NP_000521.2:p.Ser9=
NM_001315491.2:c.26G=	NP_001302420.1:p.Ser9=