Canonical Allele Identifier: CA343348492

Gene: MPZ

Linked Data

• ClinVar Variation Id: 637361
• ClinVar RCV Id: RCV000789498
• dbSNP Id: rs1456458087
• COSMIC: COSM3788971 ; COSM3788972
• MyVariant Identifiers: chr1:g.161276525G>A (hg19) ; chr1:g.161306735G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306735G>A , CM000663.2:g.161306735G>A	GRCh38
NC_000001.10:g.161276525G>A , CM000663.1:g.161276525G>A	GRCh37
NC_000001.9:g.159543149G>A	NCBI36
NG_008055.1:g.8238C>T , LRG_256:g.8238C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.367+54C>T	ENSP00000488104.2:n.367+54C>T
ENST00000533357.5:c.421C>T MANE Select	ENSP00000432943.1:p.Gln141Ter
ENST00000672287.2:c.-168C>T	ENSP00000499818.2:n.-168C>T
ENST00000672602.2:c.421C>T	ENSP00000500814.2:p.Gln141Ter
ENST00000674861.1:n.484C>T
ENST00000463290.5:c.421C>T	ENSP00000431538.1:p.Gln141Ter
ENST00000491222.5:c.-168C>T	ENSP00000431441.1:n.-168C>T
ENST00000526189.2:c.111+54C>T
ENST00000533357.4:c.421C>T	ENSP00000432943.1:p.Gln141Ter
NM_000530.6:c.421C>T , LRG_256t1:c.421C>T	NP_000521.2:p.Gln141Ter
NM_000530.7:c.421C>T	NP_000521.2:p.Gln141Ter
NM_001315491.1:c.421C>T	NP_001302420.1:p.Gln141Ter
XM_017001321.2:c.451C>T	XP_016856810.1:p.Gln151Ter
NM_000530.8:c.421C>T MANE Select	NP_000521.2:p.Gln141Ter
NM_001315491.2:c.421C>T	NP_001302420.1:p.Gln141Ter