Canonical Allele Identifier: CA1210220

Gene: MPZ

Linked Data

• ClinVar Variation Id: 917383
• ClinVar RCV Id: RCV001174329
• dbSNP Id: rs753575261
• ExAC: 1:161277108 G / A
• gnomAD v2: 1-161277108-G-A
• gnomAD v4: 1-161307318-G-A
• MyVariant Identifiers: chr1:g.161277108G>A (hg19) ; chr1:g.161307318G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161307318G>A , CM000663.2:g.161307318G>A	GRCh38
NC_000001.10:g.161277108G>A , CM000663.1:g.161277108G>A	GRCh37
NC_000001.9:g.159543732G>A	NCBI36
NG_008055.1:g.7655C>T , LRG_256:g.7655C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000526189.3:c.174C>T	ENSP00000488104.2:p.Val58=
ENST00000533357.5:c.174C>T MANE Select	ENSP00000432943.1:p.Val58=
ENST00000672287.2:c.-415C>T	ENSP00000499818.2:n.-415C>T
ENST00000672602.2:c.174C>T	ENSP00000500814.2:p.Val58=
ENST00000674861.1:n.237C>T
ENST00000463290.5:c.174C>T	ENSP00000431538.1:p.Val58=
ENST00000491222.5:c.-415C>T	ENSP00000431441.1:n.-415C>T
ENST00000533357.4:c.174C>T	ENSP00000432943.1:p.Val58=
NM_000530.6:c.174C>T , LRG_256t1:c.174C>T	NP_000521.2:p.Val58=
NM_000530.7:c.174C>T	NP_000521.2:p.Val58=
NM_001315491.1:c.174C>T	NP_001302420.1:p.Val58=
XM_017001321.2:c.204C>T	XP_016856810.1:p.Val68=
NM_000530.8:c.174C>T MANE Select	NP_000521.2:p.Val58=
NM_001315491.2:c.174C>T	NP_001302420.1:p.Val58=