Canonical Allele Identifier: CA1202690664

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161307320C= , CM000663.2:g.161307320C=	GRCh38
NC_000001.10:g.161277110C= , CM000663.1:g.161277110C=	GRCh37
NC_000001.9:g.159543734C=	NCBI36
NG_008055.1:g.7653G= , LRG_256:g.7653G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000526189.3:c.172G=	ENSP00000488104.2:p.Val58=
ENST00000533357.5:c.172G= MANE Select	ENSP00000432943.1:p.Val58=
ENST00000672287.2:c.-417G=	ENSP00000499818.2:n.-417G=
ENST00000672602.2:c.172G=	ENSP00000500814.2:p.Val58=
ENST00000674861.1:n.235G=
ENST00000463290.5:c.172G=	ENSP00000431538.1:p.Val58=
ENST00000491222.5:c.-417G=	ENSP00000431441.1:n.-417G=
ENST00000533357.4:c.172G=	ENSP00000432943.1:p.Val58=
NM_000530.6:c.172G= , LRG_256t1:c.172G=	NP_000521.2:p.Val58=
NM_000530.7:c.172G=	NP_000521.2:p.Val58=
NM_001315491.1:c.172G=	NP_001302420.1:p.Val58=
XM_017001321.2:c.202G=	XP_016856810.1:p.Val68=
NM_000530.8:c.172G= MANE Select	NP_000521.2:p.Val58=
NM_001315491.2:c.172G=	NP_001302420.1:p.Val58=