Canonical Allele Identifier: CA343348654

Gene: MPZ

Linked Data

• ClinVar Variation Id: 1685953
• ClinVar RCV Id: RCV002250120
• dbSNP Id: rs1571818775
• MyVariant Identifiers: chr1:g.161276545T>A (hg19) ; chr1:g.161306755T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306755T>A , CM000663.2:g.161306755T>A	GRCh38
NC_000001.10:g.161276545T>A , CM000663.1:g.161276545T>A	GRCh37
NC_000001.9:g.159543169T>A	NCBI36
NG_008055.1:g.8218A>T , LRG_256:g.8218A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000526189.3:c.367+34A>T	ENSP00000488104.2:n.367+34A>T
ENST00000533357.5:c.401A>T MANE Select	ENSP00000432943.1:p.Asp134Val
ENST00000672287.2:c.-188A>T	ENSP00000499818.2:n.-188A>T
ENST00000672602.2:c.401A>T	ENSP00000500814.2:p.Asp134Val
ENST00000674861.1:n.464A>T
ENST00000463290.5:c.401A>T	ENSP00000431538.1:p.Asp134Val
ENST00000491222.5:c.-188A>T	ENSP00000431441.1:n.-188A>T
ENST00000526189.2:c.111+34A>T
ENST00000533357.4:c.401A>T	ENSP00000432943.1:p.Asp134Val
NM_000530.6:c.401A>T , LRG_256t1:c.401A>T	NP_000521.2:p.Asp134Val
NM_000530.7:c.401A>T	NP_000521.2:p.Asp134Val
NM_001315491.1:c.401A>T	NP_001302420.1:p.Asp134Val
XM_017001321.2:c.431A>T	XP_016856810.1:p.Asp144Val
NM_000530.8:c.401A>T MANE Select	NP_000521.2:p.Asp134Val
NM_001315491.2:c.401A>T	NP_001302420.1:p.Asp134Val