Canonical Allele Identifier: CA1145031687

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306146G= , CM000663.2:g.161306146G=	GRCh38
NC_000001.10:g.161275936G= , CM000663.1:g.161275936G=	GRCh37
NC_000001.9:g.159542560G=	NCBI36
NG_008055.1:g.8827C= , LRG_256:g.8827C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.526C=	ENSP00000488104.2:p.His176=
ENST00000533357.5:c.607C= MANE Select	ENSP00000432943.1:p.His203=
ENST00000672287.2:c.19C=	ENSP00000499818.2:p.His7=
ENST00000672602.2:c.607C=	ENSP00000500814.2:p.His203=
ENST00000674861.1:n.670C=
ENST00000463290.5:c.607C=	ENSP00000431538.1:p.His203=
ENST00000476410.1:n.67C=
ENST00000488271.1:n.45C=
ENST00000491222.5:c.19C=	ENSP00000431441.1:p.His7=
ENST00000526189.2:c.270C=
ENST00000533357.4:c.607C=	ENSP00000432943.1:p.His203=
NM_000530.6:c.607C= , LRG_256t1:c.607C=	NP_000521.2:p.His203=
NM_000530.7:c.607C=	NP_000521.2:p.His203=
NM_001315491.1:c.607C=	NP_001302420.1:p.His203=
XM_017001321.2:c.637C=	XP_016856810.1:p.His213=
NM_000530.8:c.607C= MANE Select	NP_000521.2:p.His203=
NM_001315491.2:c.607C=	NP_001302420.1:p.His203=