Canonical Allele Identifier: CA2648774452

Gene: MPZ

Linked Data

• gnomAD v4: 1-161307518-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161307518A>T , CM000663.2:g.161307518A>T	GRCh38
NC_000001.10:g.161277308A>T , CM000663.1:g.161277308A>T	GRCh37
NC_000001.9:g.159543932A>T	NCBI36
NG_008055.1:g.7455T>A , LRG_256:g.7455T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.68-94T>A	ENSP00000488104.2:n.68-94T>A
ENST00000533357.5:c.68-94T>A MANE Select	ENSP00000432943.1:n.68-94T>A
ENST00000672602.2:c.68-94T>A	ENSP00000500814.2:n.68-94T>A
ENST00000674861.1:n.131-94T>A
ENST00000463290.5:c.68-94T>A	ENSP00000431538.1:n.68-94T>A
ENST00000533357.4:c.68-94T>A	ENSP00000432943.1:n.68-94T>A
NM_000530.6:c.68-94T>A , LRG_256t1:c.68-94T>A	NP_000521.2:n.68-94T>A
NM_000530.7:c.68-94T>A	NP_000521.2:n.68-94T>A
NM_001315491.1:c.68-94T>A	NP_001302420.1:n.68-94T>A
XM_017001321.2:c.98-94T>A	XP_016856810.1:n.98-94T>A
NM_000530.8:c.68-94T>A MANE Select	NP_000521.2:n.68-94T>A
NM_001315491.2:c.68-94T>A	NP_001302420.1:n.68-94T>A