Canonical Allele Identifier: CA10689099

Gene: MPZ

Linked Data

• ClinVar Variation Id: 683190
• ClinVar RCV Id: RCV000843343
• dbSNP Id: rs6685495
• gnomAD v2: 1-161276376-G-A
• gnomAD v3: 1-161306586-G-A
• gnomAD v4: 1-161306586-G-A
• MyVariant Identifiers: chr1:g.161276376G>A (hg19) ; chr1:g.161306586G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306586G>A , CM000663.2:g.161306586G>A	GRCh38
NC_000001.10:g.161276376G>A , CM000663.1:g.161276376G>A	GRCh37
NC_000001.9:g.159543000G>A	NCBI36
NG_008055.1:g.8387C>T , LRG_256:g.8387C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.368-122C>T	ENSP00000488104.2:n.368-122C>T
ENST00000533357.5:c.449-122C>T MANE Select	ENSP00000432943.1:n.449-122C>T
ENST00000672287.2:c.-140-122C>T	ENSP00000499818.2:n.-140-122C>T
ENST00000672602.2:c.449-122C>T	ENSP00000500814.2:n.449-122C>T
ENST00000674861.1:n.512-122C>T
ENST00000463290.5:c.449-122C>T	ENSP00000431538.1:n.449-122C>T
ENST00000491222.5:c.-140-122C>T	ENSP00000431441.1:n.-140-122C>T
ENST00000526189.2:c.112-122C>T
ENST00000533357.4:c.449-122C>T	ENSP00000432943.1:n.449-122C>T
NM_000530.6:c.449-122C>T , LRG_256t1:c.449-122C>T	NP_000521.2:n.449-122C>T
NM_000530.7:c.449-122C>T	NP_000521.2:n.449-122C>T
NM_001315491.1:c.449-122C>T	NP_001302420.1:n.449-122C>T
XM_017001321.2:c.479-122C>T	XP_016856810.1:n.479-122C>T
NM_000530.8:c.449-122C>T MANE Select	NP_000521.2:n.449-122C>T
NM_001315491.2:c.449-122C>T	NP_001302420.1:n.449-122C>T