Canonical Allele Identifier: CA2507834582

Gene: MPZ

Linked Data

• gnomAD v4: 1-161307601-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161307605_161307606del , CM000663.2:g.161307605_161307606del	GRCh38
NC_000001.10:g.161277395_161277396del , CM000663.1:g.161277395_161277396del	GRCh37
NC_000001.9:g.159544019_159544020del	NCBI36
NG_008055.1:g.7370_7371del , LRG_256:g.7370_7371del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.68-179_68-178del	ENSP00000488104.2:n.68-179_68-178del
ENST00000533357.5:c.68-179_68-178del MANE Select	ENSP00000432943.1:n.68-179_68-178del
ENST00000672602.2:c.68-179_68-178del	ENSP00000500814.2:n.68-179_68-178del
ENST00000674861.1:n.131-179_131-178del
ENST00000463290.5:c.68-179_68-178del	ENSP00000431538.1:n.68-179_68-178del
ENST00000533357.4:c.68-179_68-178del	ENSP00000432943.1:n.68-179_68-178del
NM_000530.6:c.68-179_68-178del , LRG_256t1:c.68-179_68-178del	NP_000521.2:n.68-179_68-178del
NM_000530.7:c.68-179_68-178del	NP_000521.2:n.68-179_68-178del
NM_001315491.1:c.68-179_68-178del	NP_001302420.1:n.68-179_68-178del
XM_017001321.2:c.98-179_98-178del	XP_016856810.1:n.98-179_98-178del
NM_000530.8:c.68-179_68-178del MANE Select	NP_000521.2:n.68-179_68-178del
NM_001315491.2:c.68-179_68-178del	NP_001302420.1:n.68-179_68-178del