Canonical Allele Identifier: CA1202688229

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306120C= , CM000663.2:g.161306120C=	GRCh38
NC_000001.10:g.161275910C= , CM000663.1:g.161275910C=	GRCh37
NC_000001.9:g.159542534C=	NCBI36
NG_008055.1:g.8853G= , LRG_256:g.8853G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.552G=	ENSP00000488104.2:p.Lys184=
ENST00000533357.5:c.633G= MANE Select	ENSP00000432943.1:p.Lys211=
ENST00000672287.2:c.45G=	ENSP00000499818.2:p.Lys15=
ENST00000672602.2:c.633G=	ENSP00000500814.2:p.Lys211=
ENST00000674861.1:n.696G=
ENST00000463290.5:c.633G=	ENSP00000431538.1:p.Lys211=
ENST00000476410.1:n.93G=
ENST00000488271.1:n.71G=
ENST00000491222.5:c.45G=	ENSP00000431441.1:p.Lys15=
ENST00000526189.2:c.296G=
ENST00000533357.4:c.633G=	ENSP00000432943.1:p.Lys211=
NM_000530.6:c.633G= , LRG_256t1:c.633G=	NP_000521.2:p.Lys211=
NM_000530.7:c.633G=	NP_000521.2:p.Lys211=
NM_001315491.1:c.633G=	NP_001302420.1:p.Lys211=
XM_017001321.2:c.663G=	XP_016856810.1:p.Lys221=
NM_000530.8:c.633G= MANE Select	NP_000521.2:p.Lys211=
NM_001315491.2:c.633G=	NP_001302420.1:p.Lys211=