Canonical Allele Identifier: CA343344662

Gene: MPZ

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.553C>A	ENSP00000488104.2:p.Arg185Ser
ENST00000533357.5:c.634C>A MANE Select	ENSP00000432943.1:p.Arg212Ser
ENST00000672287.2:c.46C>A	ENSP00000499818.2:p.Arg16Ser
ENST00000672602.2:c.634C>A	ENSP00000500814.2:p.Arg212Ser
ENST00000674861.1:n.697C>A
ENST00000463290.5:c.634C>A	ENSP00000431538.1:p.Arg212Ser
ENST00000476410.1:n.94C>A
ENST00000488271.1:n.72C>A
ENST00000491222.5:c.46C>A	ENSP00000431441.1:p.Arg16Ser
ENST00000526189.2:c.297C>A
ENST00000533357.4:c.634C>A	ENSP00000432943.1:p.Arg212Ser
NM_000530.6:c.634C>A , LRG_256t1:c.634C>A	NP_000521.2:p.Arg212Ser
NM_000530.7:c.634C>A	NP_000521.2:p.Arg212Ser
NM_001315491.1:c.634C>A	NP_001302420.1:p.Arg212Ser
XM_017001321.2:c.664C>A	XP_016856810.1:p.Arg222Ser
NM_000530.8:c.634C>A MANE Select	NP_000521.2:p.Arg212Ser
NM_001315491.2:c.634C>A	NP_001302420.1:p.Arg212Ser