Canonical Allele Identifier: CA343344657

Gene: MPZ

Linked Data

• MyVariant Identifiers: chr1:g.161275909G>A (hg19) ; chr1:g.161306119G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306119G>A , CM000663.2:g.161306119G>A	GRCh38
NC_000001.10:g.161275909G>A , CM000663.1:g.161275909G>A	GRCh37
NC_000001.9:g.159542533G>A	NCBI36
NG_008055.1:g.8854C>T , LRG_256:g.8854C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.553C>T	ENSP00000488104.2:p.Arg185Cys
ENST00000533357.5:c.634C>T MANE Select	ENSP00000432943.1:p.Arg212Cys
ENST00000672287.2:c.46C>T	ENSP00000499818.2:p.Arg16Cys
ENST00000672602.2:c.634C>T	ENSP00000500814.2:p.Arg212Cys
ENST00000674861.1:n.697C>T
ENST00000463290.5:c.634C>T	ENSP00000431538.1:p.Arg212Cys
ENST00000476410.1:n.94C>T
ENST00000488271.1:n.72C>T
ENST00000491222.5:c.46C>T	ENSP00000431441.1:p.Arg16Cys
ENST00000526189.2:c.297C>T
ENST00000533357.4:c.634C>T	ENSP00000432943.1:p.Arg212Cys
NM_000530.6:c.634C>T , LRG_256t1:c.634C>T	NP_000521.2:p.Arg212Cys
NM_000530.7:c.634C>T	NP_000521.2:p.Arg212Cys
NM_001315491.1:c.634C>T	NP_001302420.1:p.Arg212Cys
XM_017001321.2:c.664C>T	XP_016856810.1:p.Arg222Cys
NM_000530.8:c.634C>T MANE Select	NP_000521.2:p.Arg212Cys
NM_001315491.2:c.634C>T	NP_001302420.1:p.Arg212Cys