Canonical Allele Identifier: CA2574078169

Gene: MPZ

Linked Data

• gnomAD v4: 1-161306025-T-TGTTC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306026_161306029dup , CM000663.2:g.161306026_161306029dup	GRCh38
NC_000001.10:g.161275816_161275819dup , CM000663.1:g.161275816_161275819dup	GRCh37
NC_000001.9:g.159542440_159542443dup	NCBI36
NG_008055.1:g.8944_8947dup , LRG_256:g.8944_8947dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.565-52_565-49dup	ENSP00000488104.2:n.565-52_565-49dup
ENST00000533357.5:c.646-52_646-49dup MANE Select	ENSP00000432943.1:n.646-52_646-49dup
ENST00000672287.2:c.58-52_58-49dup	ENSP00000499818.2:n.58-52_58-49dup
ENST00000672602.2:c.646-52_646-49dup	ENSP00000500814.2:n.646-52_646-49dup
ENST00000674861.1:n.709-52_709-49dup
ENST00000463290.5:c.646-52_646-49dup	ENSP00000431538.1:n.646-52_646-49dup
ENST00000476410.1:n.184_187dup
ENST00000488271.1:n.84-52_84-49dup
ENST00000491222.5:c.58-52_58-49dup	ENSP00000431441.1:n.58-52_58-49dup
ENST00000526189.2:c.309-52_309-49dup
ENST00000533357.4:c.646-52_646-49dup	ENSP00000432943.1:n.646-52_646-49dup
NM_000530.6:c.646-52_646-49dup , LRG_256t1:c.646-52_646-49dup	NP_000521.2:n.646-52_646-49dup
NM_000530.7:c.646-52_646-49dup	NP_000521.2:n.646-52_646-49dup
NM_001315491.1:c.646-52_646-49dup	NP_001302420.1:n.646-52_646-49dup
XM_017001321.2:c.675+79_675+82dup	XP_016856810.1:n.675+79_675+82dup
NM_000530.8:c.646-52_646-49dup MANE Select	NP_000521.2:n.646-52_646-49dup
NM_001315491.2:c.646-52_646-49dup	NP_001302420.1:n.646-52_646-49dup