Canonical Allele Identifier: CA1143538426

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306165A= , CM000663.2:g.161306165A=	GRCh38
NC_000001.10:g.161275955A= , CM000663.1:g.161275955A=	GRCh37
NC_000001.9:g.159542579A=	NCBI36
NG_008055.1:g.8808T= , LRG_256:g.8808T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000530.8:c.588T= MANE Select	NP_000521.2:p.Ala196=
ENST00000533357.5:c.588T= MANE Select	ENSP00000432943.1:p.Ala196=
NM_000530.6:c.588T= , LRG_256t1:c.588T=	NP_000521.2:p.Ala196=
NM_000530.7:c.588T=	NP_000521.2:p.Ala196=
NM_001315491.1:c.588T=	NP_001302420.1:p.Ala196=
NM_001315491.2:c.588T=	NP_001302420.1:p.Ala196=
ENST00000463290.5:c.588T=	ENSP00000431538.1:p.Ala196=
ENST00000476410.1:n.48T=
ENST00000488271.1:n.26T=
ENST00000491222.5:c.-1T=	ENSP00000431441.1:n.-1T=
ENST00000526189.2:c.251T=
ENST00000526189.3:c.507T=	ENSP00000488104.2:p.Ala169=
ENST00000533357.4:c.588T=	ENSP00000432943.1:p.Ala196=
ENST00000672287.2:c.-1T=	ENSP00000499818.2:n.-1T=
ENST00000672602.2:c.588T=	ENSP00000500814.2:p.Ala196=
ENST00000674861.1:n.651T=
XM_017001321.2:c.618T=	XP_016856810.1:p.Ala206=