Canonical Allele Identifier: CA343349055

Gene: MPZ

Linked Data

• MyVariant Identifiers: chr1:g.161276584T>A (hg19) ; chr1:g.161306794T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306794T>A , CM000663.2:g.161306794T>A	GRCh38
NC_000001.10:g.161276584T>A , CM000663.1:g.161276584T>A	GRCh37
NC_000001.9:g.159543208T>A	NCBI36
NG_008055.1:g.8179A>T , LRG_256:g.8179A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000526189.3:c.362A>T	ENSP00000488104.2:p.Asp121Val
ENST00000533357.5:c.362A>T MANE Select	ENSP00000432943.1:p.Asp121Val
ENST00000672287.2:c.-227A>T	ENSP00000499818.2:n.-227A>T
ENST00000672602.2:c.362A>T	ENSP00000500814.2:p.Asp121Val
ENST00000674861.1:n.425A>T
ENST00000463290.5:c.362A>T	ENSP00000431538.1:p.Asp121Val
ENST00000491222.5:c.-227A>T	ENSP00000431441.1:n.-227A>T
ENST00000526189.2:c.106A>T
ENST00000533357.4:c.362A>T	ENSP00000432943.1:p.Asp121Val
NM_000530.6:c.362A>T , LRG_256t1:c.362A>T	NP_000521.2:p.Asp121Val
NM_000530.7:c.362A>T	NP_000521.2:p.Asp121Val
NM_001315491.1:c.362A>T	NP_001302420.1:p.Asp121Val
XM_017001321.2:c.392A>T	XP_016856810.1:p.Asp131Val
NM_000530.8:c.362A>T MANE Select	NP_000521.2:p.Asp121Val
NM_001315491.2:c.362A>T	NP_001302420.1:p.Asp121Val