Canonical Allele Identifier: CA343344713

Gene: MPZ

Linked Data

• MyVariant Identifiers: chr1:g.161275915A>T (hg19) ; chr1:g.161306125A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306125A>T , CM000663.2:g.161306125A>T	GRCh38
NC_000001.10:g.161275915A>T , CM000663.1:g.161275915A>T	GRCh37
NC_000001.9:g.159542539A>T	NCBI36
NG_008055.1:g.8848T>A , LRG_256:g.8848T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.547T>A	ENSP00000488104.2:p.Ser183Thr
ENST00000533357.5:c.628T>A MANE Select	ENSP00000432943.1:p.Ser210Thr
ENST00000672287.2:c.40T>A	ENSP00000499818.2:p.Ser14Thr
ENST00000672602.2:c.628T>A	ENSP00000500814.2:p.Ser210Thr
ENST00000674861.1:n.691T>A
ENST00000463290.5:c.628T>A	ENSP00000431538.1:p.Ser210Thr
ENST00000476410.1:n.88T>A
ENST00000488271.1:n.66T>A
ENST00000491222.5:c.40T>A	ENSP00000431441.1:p.Ser14Thr
ENST00000526189.2:c.291T>A
ENST00000533357.4:c.628T>A	ENSP00000432943.1:p.Ser210Thr
NM_000530.6:c.628T>A , LRG_256t1:c.628T>A	NP_000521.2:p.Ser210Thr
NM_000530.7:c.628T>A	NP_000521.2:p.Ser210Thr
NM_001315491.1:c.628T>A	NP_001302420.1:p.Ser210Thr
XM_017001321.2:c.658T>A	XP_016856810.1:p.Ser220Thr
NM_000530.8:c.628T>A MANE Select	NP_000521.2:p.Ser210Thr
NM_001315491.2:c.628T>A	NP_001302420.1:p.Ser210Thr