Canonical Allele Identifier: CA1202687664

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161305855C= , CM000663.2:g.161305855C=	GRCh38
NC_000001.10:g.161275645C= , CM000663.1:g.161275645C=	GRCh37
NC_000001.9:g.159542269C=	NCBI36
NG_008055.1:g.9118G= , LRG_256:g.9118G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.*21G=	ENSP00000488104.2:n.*21G=
ENST00000533357.5:c.*21G= MANE Select	ENSP00000432943.1:n.*21G=
ENST00000672287.2:c.*21G=	ENSP00000499818.2:n.*21G=
ENST00000672602.2:c.768G=	ENSP00000500814.2:p.Gly256=
ENST00000674861.1:n.831G=
ENST00000463290.5:c.*21G=	ENSP00000431538.1:n.*21G=
ENST00000476410.1:n.358G=
ENST00000488271.1:n.206G=
ENST00000491222.5:c.*21G=	ENSP00000431441.1:n.*21G=
ENST00000526189.2:c.431G=
ENST00000533357.4:c.*21G=	ENSP00000432943.1:n.*21G=
NM_000530.6:c.*21G= , LRG_256t1:c.*21G=	NP_000521.2:n.*21G=
NM_000530.7:c.*21G=	NP_000521.2:n.*21G=
NM_001315491.1:c.768G=	NP_001302420.1:p.Gly256=
XM_017001321.2:c.675+253G=	XP_016856810.1:n.675+253G=
NM_000530.8:c.*21G= MANE Select	NP_000521.2:n.*21G=
NM_001315491.2:c.768G=	NP_001302420.1:p.Gly256=