Canonical Allele Identifier: CA1202691152

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161307525A= , CM000663.2:g.161307525A=	GRCh38
NC_000001.10:g.161277315A= , CM000663.1:g.161277315A=	GRCh37
NC_000001.9:g.159543939A=	NCBI36
NG_008055.1:g.7448T= , LRG_256:g.7448T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.68-101T=	ENSP00000488104.2:n.68-101T=
ENST00000533357.5:c.68-101T= MANE Select	ENSP00000432943.1:n.68-101T=
ENST00000672602.2:c.68-101T=	ENSP00000500814.2:n.68-101T=
ENST00000674861.1:n.131-101T=
ENST00000463290.5:c.68-101T=	ENSP00000431538.1:n.68-101T=
ENST00000533357.4:c.68-101T=	ENSP00000432943.1:n.68-101T=
NM_000530.6:c.68-101T= , LRG_256t1:c.68-101T=	NP_000521.2:n.68-101T=
NM_000530.7:c.68-101T=	NP_000521.2:n.68-101T=
NM_001315491.1:c.68-101T=	NP_001302420.1:n.68-101T=
XM_017001321.2:c.98-101T=	XP_016856810.1:n.98-101T=
NM_000530.8:c.68-101T= MANE Select	NP_000521.2:n.68-101T=
NM_001315491.2:c.68-101T=	NP_001302420.1:n.68-101T=