Canonical Allele Identifier: CA1202687625

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161305824C= , CM000663.2:g.161305824C=	GRCh38
NC_000001.10:g.161275614C= , CM000663.1:g.161275614C=	GRCh37
NC_000001.9:g.159542238C=	NCBI36
NG_008055.1:g.9149G= , LRG_256:g.9149G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.*52G=	ENSP00000488104.2:n.*52G=
ENST00000533357.5:c.*52G= MANE Select	ENSP00000432943.1:n.*52G=
ENST00000672287.2:c.*52G=	ENSP00000499818.2:n.*52G=
ENST00000672602.2:c.799G=	ENSP00000500814.2:p.Gly267=
ENST00000674861.1:n.862G=
ENST00000463290.5:c.*52G=	ENSP00000431538.1:n.*52G=
ENST00000476410.1:n.389G=
ENST00000488271.1:n.237G=
ENST00000491222.5:c.*52G=	ENSP00000431441.1:n.*52G=
ENST00000526189.2:c.462G=
ENST00000533357.4:c.*52G=	ENSP00000432943.1:n.*52G=
NM_000530.6:c.*52G= , LRG_256t1:c.*52G=	NP_000521.2:n.*52G=
NM_000530.7:c.*52G=	NP_000521.2:n.*52G=
NM_001315491.1:c.799G=	NP_001302420.1:p.Gly267=
XM_017001321.2:c.675+284G=	XP_016856810.1:n.675+284G=
NM_000530.8:c.*52G= MANE Select	NP_000521.2:n.*52G=
NM_001315491.2:c.799G=	NP_001302420.1:p.Gly267=