Canonical Allele Identifier: CA343349097

Gene: MPZ

Linked Data

• MyVariant Identifiers: chr1:g.161276586A>C (hg19) ; chr1:g.161306796A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306796A>C , CM000663.2:g.161306796A>C	GRCh38
NC_000001.10:g.161276586A>C , CM000663.1:g.161276586A>C	GRCh37
NC_000001.9:g.159543210A>C	NCBI36
NG_008055.1:g.8177T>G , LRG_256:g.8177T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000526189.3:c.360T>G	ENSP00000488104.2:p.Ser120Arg
ENST00000533357.5:c.360T>G MANE Select	ENSP00000432943.1:p.Ser120Arg
ENST00000672287.2:c.-229T>G	ENSP00000499818.2:n.-229T>G
ENST00000672602.2:c.360T>G	ENSP00000500814.2:p.Ser120Arg
ENST00000674861.1:n.423T>G
ENST00000463290.5:c.360T>G	ENSP00000431538.1:p.Ser120Arg
ENST00000491222.5:c.-229T>G	ENSP00000431441.1:n.-229T>G
ENST00000526189.2:c.104T>G
ENST00000533357.4:c.360T>G	ENSP00000432943.1:p.Ser120Arg
NM_000530.6:c.360T>G , LRG_256t1:c.360T>G	NP_000521.2:p.Ser120Arg
NM_000530.7:c.360T>G	NP_000521.2:p.Ser120Arg
NM_001315491.1:c.360T>G	NP_001302420.1:p.Ser120Arg
XM_017001321.2:c.390T>G	XP_016856810.1:p.Ser130Arg
NM_000530.8:c.360T>G MANE Select	NP_000521.2:p.Ser120Arg
NM_001315491.2:c.360T>G	NP_001302420.1:p.Ser120Arg