Canonical Allele Identifier: CA1202689526

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306800T= , CM000663.2:g.161306800T=	GRCh38
NC_000001.10:g.161276590T= , CM000663.1:g.161276590T=	GRCh37
NC_000001.9:g.159543214T=	NCBI36
NG_008055.1:g.8173A= , LRG_256:g.8173A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.356A=	ENSP00000488104.2:p.Tyr119=
ENST00000533357.5:c.356A= MANE Select	ENSP00000432943.1:p.Tyr119=
ENST00000672287.2:c.-233A=	ENSP00000499818.2:n.-233A=
ENST00000672602.2:c.356A=	ENSP00000500814.2:p.Tyr119=
ENST00000674861.1:n.419A=
ENST00000463290.5:c.356A=	ENSP00000431538.1:p.Tyr119=
ENST00000491222.5:c.-233A=	ENSP00000431441.1:n.-233A=
ENST00000526189.2:c.100A=
ENST00000533357.4:c.356A=	ENSP00000432943.1:p.Tyr119=
NM_000530.6:c.356A= , LRG_256t1:c.356A=	NP_000521.2:p.Tyr119=
NM_000530.7:c.356A=	NP_000521.2:p.Tyr119=
NM_001315491.1:c.356A=	NP_001302420.1:p.Tyr119=
XM_017001321.2:c.386A=	XP_016856810.1:p.Tyr129=
NM_000530.8:c.356A= MANE Select	NP_000521.2:p.Tyr119=
NM_001315491.2:c.356A=	NP_001302420.1:p.Tyr119=