Canonical Allele Identifier: CA343348440

Gene: MPZ

Linked Data

• ClinVar Variation Id: 2815850
• ClinVar RCV Id: RCV003741779
• MyVariant Identifiers: chr1:g.161276522C>T (hg19) ; chr1:g.161306732C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306732C>T , CM000663.2:g.161306732C>T	GRCh38
NC_000001.10:g.161276522C>T , CM000663.1:g.161276522C>T	GRCh37
NC_000001.9:g.159543146C>T	NCBI36
NG_008055.1:g.8241G>A , LRG_256:g.8241G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.367+57G>A	ENSP00000488104.2:n.367+57G>A
ENST00000533357.5:c.424G>A MANE Select	ENSP00000432943.1:p.Val142Ile
ENST00000672287.2:c.-165G>A	ENSP00000499818.2:n.-165G>A
ENST00000672602.2:c.424G>A	ENSP00000500814.2:p.Val142Ile
ENST00000674861.1:n.487G>A
ENST00000463290.5:c.424G>A	ENSP00000431538.1:p.Val142Ile
ENST00000491222.5:c.-165G>A	ENSP00000431441.1:n.-165G>A
ENST00000526189.2:c.111+57G>A
ENST00000533357.4:c.424G>A	ENSP00000432943.1:p.Val142Ile
NM_000530.6:c.424G>A , LRG_256t1:c.424G>A	NP_000521.2:p.Val142Ile
NM_000530.7:c.424G>A	NP_000521.2:p.Val142Ile
NM_001315491.1:c.424G>A	NP_001302420.1:p.Val142Ile
XM_017001321.2:c.454G>A	XP_016856810.1:p.Val152Ile
NM_000530.8:c.424G>A MANE Select	NP_000521.2:p.Val142Ile
NM_001315491.2:c.424G>A	NP_001302420.1:p.Val142Ile