Canonical Allele Identifier: CA343350426

Gene: MPZ

Linked Data

• ClinVar Variation Id: 2117747
• ClinVar RCV Id: RCV003030129
• MyVariant Identifiers: chr1:g.161277073G>T (hg19) ; chr1:g.161307283G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161307283G>T , CM000663.2:g.161307283G>T	GRCh38
NC_000001.10:g.161277073G>T , CM000663.1:g.161277073G>T	GRCh37
NC_000001.9:g.159543697G>T	NCBI36
NG_008055.1:g.7690C>A , LRG_256:g.7690C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.209C>A	ENSP00000488104.2:p.Pro70His
ENST00000533357.5:c.209C>A MANE Select	ENSP00000432943.1:p.Pro70His
ENST00000672287.2:c.-380C>A	ENSP00000499818.2:n.-380C>A
ENST00000672602.2:c.209C>A	ENSP00000500814.2:p.Pro70His
ENST00000674861.1:n.272C>A
ENST00000463290.5:c.209C>A	ENSP00000431538.1:p.Pro70His
ENST00000491222.5:c.-380C>A	ENSP00000431441.1:n.-380C>A
ENST00000533357.4:c.209C>A	ENSP00000432943.1:p.Pro70His
NM_000530.6:c.209C>A , LRG_256t1:c.209C>A	NP_000521.2:p.Pro70His
NM_000530.7:c.209C>A	NP_000521.2:p.Pro70His
NM_001315491.1:c.209C>A	NP_001302420.1:p.Pro70His
XM_017001321.2:c.239C>A	XP_016856810.1:p.Pro80His
NM_000530.8:c.209C>A MANE Select	NP_000521.2:p.Pro70His
NM_001315491.2:c.209C>A	NP_001302420.1:p.Pro70His