Canonical Allele Identifier: CA343351325
Gene: MPZ HGNC NCBI

Linked Data

dbSNP Id: rs760227243

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161307358C>A , CM000663.2:g.161307358C>A GRCh38
NC_000001.10:g.161277148C>A , CM000663.1:g.161277148C>A GRCh37
NC_000001.9:g.159543772C>A NCBI36
NG_008055.1:g.7615G>T , LRG_256:g.7615G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000526189.3:c.134G>T ENSP00000488104.2:p.Arg45Leu
ENST00000533357.5:c.134G>T MANE Select ENSP00000432943.1:p.Arg45Leu
ENST00000672287.2:c.-455G>T ENSP00000499818.2:n.-455G>T
ENST00000672602.2:c.134G>T ENSP00000500814.2:p.Arg45Leu
ENST00000674861.1:n.197G>T
ENST00000463290.5:c.134G>T ENSP00000431538.1:p.Arg45Leu
ENST00000491222.5:c.-455G>T ENSP00000431441.1:n.-455G>T
ENST00000533357.4:c.134G>T ENSP00000432943.1:p.Arg45Leu
NM_000530.6:c.134G>T , LRG_256t1:c.134G>T NP_000521.2:p.Arg45Leu
NM_000530.7:c.134G>T NP_000521.2:p.Arg45Leu
NM_001315491.1:c.134G>T NP_001302420.1:p.Arg45Leu
XM_017001321.2:c.164G>T XP_016856810.1:p.Arg55Leu
NM_000530.8:c.134G>T MANE Select NP_000521.2:p.Arg45Leu
NM_001315491.2:c.134G>T NP_001302420.1:p.Arg45Leu