Canonical Allele Identifier: CA1202689120

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306712T= , CM000663.2:g.161306712T=	GRCh38
NC_000001.10:g.161276502T= , CM000663.1:g.161276502T=	GRCh37
NC_000001.9:g.159543126T=	NCBI36
NG_008055.1:g.8261A= , LRG_256:g.8261A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.367+77A=	ENSP00000488104.2:n.367+77A=
ENST00000533357.5:c.444A= MANE Select	ENSP00000432943.1:p.Glu148=
ENST00000672287.2:c.-145A=	ENSP00000499818.2:n.-145A=
ENST00000672602.2:c.444A=	ENSP00000500814.2:p.Glu148=
ENST00000674861.1:n.507A=
ENST00000463290.5:c.444A=	ENSP00000431538.1:p.Glu148=
ENST00000491222.5:c.-145A=	ENSP00000431441.1:n.-145A=
ENST00000526189.2:c.111+77A=
ENST00000533357.4:c.444A=	ENSP00000432943.1:p.Glu148=
NM_000530.6:c.444A= , LRG_256t1:c.444A=	NP_000521.2:p.Glu148=
NM_000530.7:c.444A=	NP_000521.2:p.Glu148=
NM_001315491.1:c.444A=	NP_001302420.1:p.Glu148=
XM_017001321.2:c.474A=	XP_016856810.1:p.Glu158=
NM_000530.8:c.444A= MANE Select	NP_000521.2:p.Glu148=
NM_001315491.2:c.444A=	NP_001302420.1:p.Glu148=