Canonical Allele Identifier: CA2648774385

Gene: MPZ

Linked Data

• gnomAD v4: 1-161307448-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161307449del , CM000663.2:g.161307449del	GRCh38
NC_000001.10:g.161277239del , CM000663.1:g.161277239del	GRCh37
NC_000001.9:g.159543863del	NCBI36
NG_008055.1:g.7524del , LRG_256:g.7524del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.68-25del	ENSP00000488104.2:n.68-25del
ENST00000533357.5:c.68-25del MANE Select	ENSP00000432943.1:n.68-25del
ENST00000672287.2:c.-546del	ENSP00000499818.2:n.-546del
ENST00000672602.2:c.68-25del	ENSP00000500814.2:n.68-25del
ENST00000674861.1:n.131-25del
ENST00000463290.5:c.68-25del	ENSP00000431538.1:n.68-25del
ENST00000491222.5:c.-546del	ENSP00000431441.1:n.-546del
ENST00000533357.4:c.68-25del	ENSP00000432943.1:n.68-25del
NM_000530.6:c.68-25del , LRG_256t1:c.68-25del	NP_000521.2:n.68-25del
NM_000530.7:c.68-25del	NP_000521.2:n.68-25del
NM_001315491.1:c.68-25del	NP_001302420.1:n.68-25del
XM_017001321.2:c.98-25del	XP_016856810.1:n.98-25del
NM_000530.8:c.68-25del MANE Select	NP_000521.2:n.68-25del
NM_001315491.2:c.68-25del	NP_001302420.1:n.68-25del