Canonical Allele Identifier: CA1202689183

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306728G= , CM000663.2:g.161306728G=	GRCh38
NC_000001.10:g.161276518G= , CM000663.1:g.161276518G=	GRCh37
NC_000001.9:g.159543142G=	NCBI36
NG_008055.1:g.8245C= , LRG_256:g.8245C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.367+61C=	ENSP00000488104.2:n.367+61C=
ENST00000533357.5:c.428C= MANE Select	ENSP00000432943.1:p.Thr143=
ENST00000672287.2:c.-161C=	ENSP00000499818.2:n.-161C=
ENST00000672602.2:c.428C=	ENSP00000500814.2:p.Thr143=
ENST00000674861.1:n.491C=
ENST00000463290.5:c.428C=	ENSP00000431538.1:p.Thr143=
ENST00000491222.5:c.-161C=	ENSP00000431441.1:n.-161C=
ENST00000526189.2:c.111+61C=
ENST00000533357.4:c.428C=	ENSP00000432943.1:p.Thr143=
NM_000530.6:c.428C= , LRG_256t1:c.428C=	NP_000521.2:p.Thr143=
NM_000530.7:c.428C=	NP_000521.2:p.Thr143=
NM_001315491.1:c.428C=	NP_001302420.1:p.Thr143=
XM_017001321.2:c.458C=	XP_016856810.1:p.Thr153=
NM_000530.8:c.428C= MANE Select	NP_000521.2:p.Thr143=
NM_001315491.2:c.428C=	NP_001302420.1:p.Thr143=