Canonical Allele Identifier: CA16609894

Gene: MPZ

Linked Data

• ClinVar Variation Id: 411668
• ClinVar RCV Id: RCV000477088 ; RCV000790084
• dbSNP Id: rs1060503420
• MyVariant Identifiers: chr1:g.161276621C>T (hg19) ; chr1:g.161306831C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306831C>T , CM000663.2:g.161306831C>T	GRCh38
NC_000001.10:g.161276621C>T , CM000663.1:g.161276621C>T	GRCh37
NC_000001.9:g.159543245C>T	NCBI36
NG_008055.1:g.8142G>A , LRG_256:g.8142G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.325G>A	ENSP00000488104.2:p.Asp109Asn
ENST00000533357.5:c.325G>A MANE Select	ENSP00000432943.1:p.Asp109Asn
ENST00000672287.2:c.-264G>A	ENSP00000499818.2:n.-264G>A
ENST00000672602.2:c.325G>A	ENSP00000500814.2:p.Asp109Asn
ENST00000674861.1:n.388G>A
ENST00000463290.5:c.325G>A	ENSP00000431538.1:p.Asp109Asn
ENST00000491222.5:c.-264G>A	ENSP00000431441.1:n.-264G>A
ENST00000526189.2:c.69G>A
ENST00000533357.4:c.325G>A	ENSP00000432943.1:p.Asp109Asn
NM_000530.6:c.325G>A , LRG_256t1:c.325G>A	NP_000521.2:p.Asp109Asn
NM_000530.7:c.325G>A	NP_000521.2:p.Asp109Asn
NM_001315491.1:c.325G>A	NP_001302420.1:p.Asp109Asn
XM_017001321.2:c.355G>A	XP_016856810.1:p.Asp119Asn
NM_000530.8:c.325G>A MANE Select	NP_000521.2:p.Asp109Asn
NM_001315491.2:c.325G>A	NP_001302420.1:p.Asp109Asn