Canonical Allele Identifier: CA2648774549

Gene: MPZ

Linked Data

• gnomAD v4: 1-161307585-CAGATG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161307588_161307592del , CM000663.2:g.161307588_161307592del	GRCh38
NC_000001.10:g.161277378_161277382del , CM000663.1:g.161277378_161277382del	GRCh37
NC_000001.9:g.159544002_159544006del	NCBI36
NG_008055.1:g.7383_7387del , LRG_256:g.7383_7387del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.68-166_68-162del	ENSP00000488104.2:n.68-166_68-162del
ENST00000533357.5:c.68-166_68-162del MANE Select	ENSP00000432943.1:n.68-166_68-162del
ENST00000672602.2:c.68-166_68-162del	ENSP00000500814.2:n.68-166_68-162del
ENST00000674861.1:n.131-166_131-162del
ENST00000463290.5:c.68-166_68-162del	ENSP00000431538.1:n.68-166_68-162del
ENST00000533357.4:c.68-166_68-162del	ENSP00000432943.1:n.68-166_68-162del
NM_000530.6:c.68-166_68-162del , LRG_256t1:c.68-166_68-162del	NP_000521.2:n.68-166_68-162del
NM_000530.7:c.68-166_68-162del	NP_000521.2:n.68-166_68-162del
NM_001315491.1:c.68-166_68-162del	NP_001302420.1:n.68-166_68-162del
XM_017001321.2:c.98-166_98-162del	XP_016856810.1:n.98-166_98-162del
NM_000530.8:c.68-166_68-162del MANE Select	NP_000521.2:n.68-166_68-162del
NM_001315491.2:c.68-166_68-162del	NP_001302420.1:n.68-166_68-162del