Canonical Allele Identifier: CA1202689499

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306791T= , CM000663.2:g.161306791T=	GRCh38
NC_000001.10:g.161276581T= , CM000663.1:g.161276581T=	GRCh37
NC_000001.9:g.159543205T=	NCBI36
NG_008055.1:g.8182A= , LRG_256:g.8182A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000526189.3:c.365A=	ENSP00000488104.2:p.Asn122=
ENST00000533357.5:c.365A= MANE Select	ENSP00000432943.1:p.Asn122=
ENST00000672287.2:c.-224A=	ENSP00000499818.2:n.-224A=
ENST00000672602.2:c.365A=	ENSP00000500814.2:p.Asn122=
ENST00000674861.1:n.428A=
ENST00000463290.5:c.365A=	ENSP00000431538.1:p.Asn122=
ENST00000491222.5:c.-224A=	ENSP00000431441.1:n.-224A=
ENST00000526189.2:c.109A=
ENST00000533357.4:c.365A=	ENSP00000432943.1:p.Asn122=
NM_000530.6:c.365A= , LRG_256t1:c.365A=	NP_000521.2:p.Asn122=
NM_000530.7:c.365A=	NP_000521.2:p.Asn122=
NM_001315491.1:c.365A=	NP_001302420.1:p.Asn122=
XM_017001321.2:c.395A=	XP_016856810.1:p.Asn132=
NM_000530.8:c.365A= MANE Select	NP_000521.2:p.Asn122=
NM_001315491.2:c.365A=	NP_001302420.1:p.Asn122=