Canonical Allele Identifier: CA421405070

Gene: MPZ

Linked Data

• dbSNP Id: rs1571818696
• MyVariant Identifiers: chr1:g.161276529G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306739G>C , CM000663.2:g.161306739G>C	GRCh38
NC_000001.10:g.161276529G>C , CM000663.1:g.161276529G>C	GRCh37
NC_000001.9:g.159543153G>C	NCBI36
NG_008055.1:g.8234C>G , LRG_256:g.8234C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.367+50C>G	ENSP00000488104.2:n.367+50C>G
ENST00000533357.5:c.417C>G MANE Select	ENSP00000432943.1:p.Thr139=
ENST00000672287.2:c.-172C>G	ENSP00000499818.2:n.-172C>G
ENST00000672602.2:c.417C>G	ENSP00000500814.2:p.Thr139=
ENST00000674861.1:n.480C>G
ENST00000463290.5:c.417C>G	ENSP00000431538.1:p.Thr139=
ENST00000491222.5:c.-172C>G	ENSP00000431441.1:n.-172C>G
ENST00000526189.2:c.111+50C>G
ENST00000533357.4:c.417C>G	ENSP00000432943.1:p.Thr139=
NM_000530.6:c.417C>G , LRG_256t1:c.417C>G	NP_000521.2:p.Thr139=
NM_000530.7:c.417C>G	NP_000521.2:p.Thr139=
NM_001315491.1:c.417C>G	NP_001302420.1:p.Thr139=
XM_017001321.2:c.447C>G	XP_016856810.1:p.Thr149=
NM_000530.8:c.417C>G MANE Select	NP_000521.2:p.Thr139=
NM_001315491.2:c.417C>G	NP_001302420.1:p.Thr139=