Canonical Allele Identifier: CA343344629

Gene: MPZ

Linked Data

• MyVariant Identifiers: chr1:g.161275905C>G (hg19) ; chr1:g.161306115C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306115C>G , CM000663.2:g.161306115C>G	GRCh38
NC_000001.10:g.161275905C>G , CM000663.1:g.161275905C>G	GRCh37
NC_000001.9:g.159542529C>G	NCBI36
NG_008055.1:g.8858G>C , LRG_256:g.8858G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.557G>C	ENSP00000488104.2:p.Gly186Ala
ENST00000533357.5:c.638G>C MANE Select	ENSP00000432943.1:p.Gly213Ala
ENST00000672287.2:c.50G>C	ENSP00000499818.2:p.Gly17Ala
ENST00000672602.2:c.638G>C	ENSP00000500814.2:p.Gly213Ala
ENST00000674861.1:n.701G>C
ENST00000463290.5:c.638G>C	ENSP00000431538.1:p.Gly213Ala
ENST00000476410.1:n.98G>C
ENST00000488271.1:n.76G>C
ENST00000491222.5:c.50G>C	ENSP00000431441.1:p.Gly17Ala
ENST00000526189.2:c.301G>C
ENST00000533357.4:c.638G>C	ENSP00000432943.1:p.Gly213Ala
NM_000530.6:c.638G>C , LRG_256t1:c.638G>C	NP_000521.2:p.Gly213Ala
NM_000530.7:c.638G>C	NP_000521.2:p.Gly213Ala
NM_001315491.1:c.638G>C	NP_001302420.1:p.Gly213Ala
XM_017001321.2:c.668G>C	XP_016856810.1:p.Gly223Ala
NM_000530.8:c.638G>C MANE Select	NP_000521.2:p.Gly213Ala
NM_001315491.2:c.638G>C	NP_001302420.1:p.Gly213Ala