Canonical Allele Identifier: CA343344809

Gene: MPZ

Linked Data

• ClinVar Variation Id: 2849285
• ClinVar RCV Id: RCV003742155
• MyVariant Identifiers: chr1:g.161275929G>A (hg19) ; chr1:g.161306139G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306139G>A , CM000663.2:g.161306139G>A	GRCh38
NC_000001.10:g.161275929G>A , CM000663.1:g.161275929G>A	GRCh37
NC_000001.9:g.159542553G>A	NCBI36
NG_008055.1:g.8834C>T , LRG_256:g.8834C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.533C>T	ENSP00000488104.2:p.Pro178Leu
ENST00000533357.5:c.614C>T MANE Select	ENSP00000432943.1:p.Pro205Leu
ENST00000672287.2:c.26C>T	ENSP00000499818.2:p.Pro9Leu
ENST00000672602.2:c.614C>T	ENSP00000500814.2:p.Pro205Leu
ENST00000674861.1:n.677C>T
ENST00000463290.5:c.614C>T	ENSP00000431538.1:p.Pro205Leu
ENST00000476410.1:n.74C>T
ENST00000488271.1:n.52C>T
ENST00000491222.5:c.26C>T	ENSP00000431441.1:p.Pro9Leu
ENST00000526189.2:c.277C>T
ENST00000533357.4:c.614C>T	ENSP00000432943.1:p.Pro205Leu
NM_000530.6:c.614C>T , LRG_256t1:c.614C>T	NP_000521.2:p.Pro205Leu
NM_000530.7:c.614C>T	NP_000521.2:p.Pro205Leu
NM_001315491.1:c.614C>T	NP_001302420.1:p.Pro205Leu
XM_017001321.2:c.644C>T	XP_016856810.1:p.Pro215Leu
NM_000530.8:c.614C>T MANE Select	NP_000521.2:p.Pro205Leu
NM_001315491.2:c.614C>T	NP_001302420.1:p.Pro205Leu