Canonical Allele Identifier: CA1202689089

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306689_161306690delinsTC , CM000663.2:g.161306689_161306690delinsTC	GRCh38
NC_000001.10:g.161276479_161276480delinsTC , CM000663.1:g.161276479_161276480delinsTC	GRCh37
NC_000001.9:g.159543103_159543104delinsTC	NCBI36
NG_008055.1:g.8283_8284delinsGA , LRG_256:g.8283_8284delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.367+99_367+100delinsGA	ENSP00000488104.2:n.367+99_367+100delinsGA
ENST00000533357.5:c.448+18_448+19delinsGA MANE Select	ENSP00000432943.1:n.448+18_448+19delinsGA
ENST00000672287.2:c.-141+18_-141+19delinsGA	ENSP00000499818.2:n.-141+18_-141+19delinsGA
ENST00000672602.2:c.448+18_448+19delinsGA	ENSP00000500814.2:n.448+18_448+19delinsGA
ENST00000674861.1:n.511+18_511+19delinsGA
ENST00000463290.5:c.448+18_448+19delinsGA	ENSP00000431538.1:n.448+18_448+19delinsGA
ENST00000491222.5:c.-141+18_-141+19delinsGA	ENSP00000431441.1:n.-141+18_-141+19delinsGA
ENST00000526189.2:c.111+99_111+100delinsGA
ENST00000533357.4:c.448+18_448+19delinsGA	ENSP00000432943.1:n.448+18_448+19delinsGA
NM_000530.6:c.448+18_448+19delinsGA , LRG_256t1:c.448+18_448+19delinsGA	NP_000521.2:n.448+18_448+19delinsGA
NM_000530.7:c.448+18_448+19delinsGA	NP_000521.2:n.448+18_448+19delinsGA
NM_001315491.1:c.448+18_448+19delinsGA	NP_001302420.1:n.448+18_448+19delinsGA
XM_017001321.2:c.478+18_478+19delinsGA	XP_016856810.1:n.478+18_478+19delinsGA
NM_000530.8:c.448+18_448+19delinsGA MANE Select	NP_000521.2:n.448+18_448+19delinsGA
NM_001315491.2:c.448+18_448+19delinsGA	NP_001302420.1:n.448+18_448+19delinsGA