Canonical Allele Identifier: CA1202689365

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306764T= , CM000663.2:g.161306764T=	GRCh38
NC_000001.10:g.161276554T= , CM000663.1:g.161276554T=	GRCh37
NC_000001.9:g.159543178T=	NCBI36
NG_008055.1:g.8209A= , LRG_256:g.8209A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.367+25A=	ENSP00000488104.2:n.367+25A=
ENST00000533357.5:c.392A= MANE Select	ENSP00000432943.1:p.Asn131=
ENST00000672287.2:c.-197A=	ENSP00000499818.2:n.-197A=
ENST00000672602.2:c.392A=	ENSP00000500814.2:p.Asn131=
ENST00000674861.1:n.455A=
ENST00000463290.5:c.392A=	ENSP00000431538.1:p.Asn131=
ENST00000491222.5:c.-197A=	ENSP00000431441.1:n.-197A=
ENST00000526189.2:c.111+25A=
ENST00000533357.4:c.392A=	ENSP00000432943.1:p.Asn131=
NM_000530.6:c.392A= , LRG_256t1:c.392A=	NP_000521.2:p.Asn131=
NM_000530.7:c.392A=	NP_000521.2:p.Asn131=
NM_001315491.1:c.392A=	NP_001302420.1:p.Asn131=
XM_017001321.2:c.422A=	XP_016856810.1:p.Asn141=
NM_000530.8:c.392A= MANE Select	NP_000521.2:p.Asn131=
NM_001315491.2:c.392A=	NP_001302420.1:p.Asn131=