Canonical Allele Identifier: CA2648773391

Gene: MPZ

Linked Data

• gnomAD v4: 1-161306626-TGCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306627_161306629del , CM000663.2:g.161306627_161306629del	GRCh38
NC_000001.10:g.161276417_161276419del , CM000663.1:g.161276417_161276419del	GRCh37
NC_000001.9:g.159543041_159543043del	NCBI36
NG_008055.1:g.8344_8346del , LRG_256:g.8344_8346del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.367+160_368-163del	ENSP00000488104.2:n.367+160_368-163del
ENST00000533357.5:c.448+79_448+81del MANE Select	ENSP00000432943.1:n.448+79_448+81del
ENST00000672287.2:c.-141+79_-141+81del	ENSP00000499818.2:n.-141+79_-141+81del
ENST00000672602.2:c.448+79_448+81del	ENSP00000500814.2:n.448+79_448+81del
ENST00000674861.1:n.511+79_511+81del
ENST00000463290.5:c.448+79_448+81del	ENSP00000431538.1:n.448+79_448+81del
ENST00000491222.5:c.-141+79_-141+81del	ENSP00000431441.1:n.-141+79_-141+81del
ENST00000526189.2:c.111+160_112-163del
ENST00000533357.4:c.448+79_448+81del	ENSP00000432943.1:n.448+79_448+81del
NM_000530.6:c.448+79_448+81del , LRG_256t1:c.448+79_448+81del	NP_000521.2:n.448+79_448+81del
NM_000530.7:c.448+79_448+81del	NP_000521.2:n.448+79_448+81del
NM_001315491.1:c.448+79_448+81del	NP_001302420.1:n.448+79_448+81del
XM_017001321.2:c.478+79_478+81del	XP_016856810.1:n.478+79_478+81del
NM_000530.8:c.448+79_448+81del MANE Select	NP_000521.2:n.448+79_448+81del
NM_001315491.2:c.448+79_448+81del	NP_001302420.1:n.448+79_448+81del