Canonical Allele Identifier: CA421404287

Gene: MPZ

Linked Data

• dbSNP Id: rs1558153432
• gnomAD v4: 1-161306114-C-T
• MyVariant Identifiers: chr1:g.161275904C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306114C>T , CM000663.2:g.161306114C>T	GRCh38
NC_000001.10:g.161275904C>T , CM000663.1:g.161275904C>T	GRCh37
NC_000001.9:g.159542528C>T	NCBI36
NG_008055.1:g.8859G>A , LRG_256:g.8859G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.558G>A	ENSP00000488104.2:p.Gly186=
ENST00000533357.5:c.639G>A MANE Select	ENSP00000432943.1:p.Gly213=
ENST00000672287.2:c.51G>A	ENSP00000499818.2:p.Gly17=
ENST00000672602.2:c.639G>A	ENSP00000500814.2:p.Gly213=
ENST00000674861.1:n.702G>A
ENST00000463290.5:c.639G>A	ENSP00000431538.1:p.Gly213=
ENST00000476410.1:n.99G>A
ENST00000488271.1:n.77G>A
ENST00000491222.5:c.51G>A	ENSP00000431441.1:p.Gly17=
ENST00000526189.2:c.302G>A
ENST00000533357.4:c.639G>A	ENSP00000432943.1:p.Gly213=
NM_000530.6:c.639G>A , LRG_256t1:c.639G>A	NP_000521.2:p.Gly213=
NM_000530.7:c.639G>A	NP_000521.2:p.Gly213=
NM_001315491.1:c.639G>A	NP_001302420.1:p.Gly213=
XM_017001321.2:c.669G>A	XP_016856810.1:p.Gly223=
NM_000530.8:c.639G>A MANE Select	NP_000521.2:p.Gly213=
NM_001315491.2:c.639G>A	NP_001302420.1:p.Gly213=