Canonical Allele Identifier: CA2648774520

Gene: MPZ

Linked Data

• gnomAD v4: 1-161307565-G-GAC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161307565_161307566insAC , CM000663.2:g.161307565_161307566insAC	GRCh38
NC_000001.10:g.161277355_161277356insAC , CM000663.1:g.161277355_161277356insAC	GRCh37
NC_000001.9:g.159543979_159543980insAC	NCBI36
NG_008055.1:g.7407_7408insGT , LRG_256:g.7407_7408insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.68-142_68-141insGT	ENSP00000488104.2:n.68-142_68-141insGT
ENST00000533357.5:c.68-142_68-141insGT MANE Select	ENSP00000432943.1:n.68-142_68-141insGT
ENST00000672602.2:c.68-142_68-141insGT	ENSP00000500814.2:n.68-142_68-141insGT
ENST00000674861.1:n.131-142_131-141insGT
ENST00000463290.5:c.68-142_68-141insGT	ENSP00000431538.1:n.68-142_68-141insGT
ENST00000533357.4:c.68-142_68-141insGT	ENSP00000432943.1:n.68-142_68-141insGT
NM_000530.6:c.68-142_68-141insGT , LRG_256t1:c.68-142_68-141insGT	NP_000521.2:n.68-142_68-141insGT
NM_000530.7:c.68-142_68-141insGT	NP_000521.2:n.68-142_68-141insGT
NM_001315491.1:c.68-142_68-141insGT	NP_001302420.1:n.68-142_68-141insGT
XM_017001321.2:c.98-142_98-141insGT	XP_016856810.1:n.98-142_98-141insGT
NM_000530.8:c.68-142_68-141insGT MANE Select	NP_000521.2:n.68-142_68-141insGT
NM_001315491.2:c.68-142_68-141insGT	NP_001302420.1:n.68-142_68-141insGT