Canonical Allele Identifier: CA1141581145

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306866T= , CM000663.2:g.161306866T=	GRCh38
NC_000001.10:g.161276656T= , CM000663.1:g.161276656T=	GRCh37
NC_000001.9:g.159543280T=	NCBI36
NG_008055.1:g.8107A= , LRG_256:g.8107A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.290A=	ENSP00000488104.2:p.Glu97=
ENST00000533357.5:c.290A= MANE Select	ENSP00000432943.1:p.Glu97=
ENST00000672287.2:c.-299A=	ENSP00000499818.2:n.-299A=
ENST00000672602.2:c.290A=	ENSP00000500814.2:p.Glu97=
ENST00000674861.1:n.353A=
ENST00000463290.5:c.290A=	ENSP00000431538.1:p.Glu97=
ENST00000491222.5:c.-299A=	ENSP00000431441.1:n.-299A=
ENST00000526189.2:c.34A=
ENST00000533357.4:c.290A=	ENSP00000432943.1:p.Glu97=
NM_000530.6:c.290A= , LRG_256t1:c.290A=	NP_000521.2:p.Glu97=
NM_000530.7:c.290A=	NP_000521.2:p.Glu97=
NM_001315491.1:c.290A=	NP_001302420.1:p.Glu97=
XM_017001321.2:c.320A=	XP_016856810.1:p.Glu107=
NM_000530.8:c.290A= MANE Select	NP_000521.2:p.Glu97=
NM_001315491.2:c.290A=	NP_001302420.1:p.Glu97=