Canonical Allele Identifier: CA2648773423

Gene: MPZ

Linked Data

• gnomAD v4: 1-161306680-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306680A>G , CM000663.2:g.161306680A>G	GRCh38
NC_000001.10:g.161276470A>G , CM000663.1:g.161276470A>G	GRCh37
NC_000001.9:g.159543094A>G	NCBI36
NG_008055.1:g.8293T>C , LRG_256:g.8293T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000526189.3:c.367+109T>C	ENSP00000488104.2:n.367+109T>C
ENST00000533357.5:c.448+28T>C MANE Select	ENSP00000432943.1:n.448+28T>C
ENST00000672287.2:c.-141+28T>C	ENSP00000499818.2:n.-141+28T>C
ENST00000672602.2:c.448+28T>C	ENSP00000500814.2:n.448+28T>C
ENST00000674861.1:n.511+28T>C
ENST00000463290.5:c.448+28T>C	ENSP00000431538.1:n.448+28T>C
ENST00000491222.5:c.-141+28T>C	ENSP00000431441.1:n.-141+28T>C
ENST00000526189.2:c.111+109T>C
ENST00000533357.4:c.448+28T>C	ENSP00000432943.1:n.448+28T>C
NM_000530.6:c.448+28T>C , LRG_256t1:c.448+28T>C	NP_000521.2:n.448+28T>C
NM_000530.7:c.448+28T>C	NP_000521.2:n.448+28T>C
NM_001315491.1:c.448+28T>C	NP_001302420.1:n.448+28T>C
XM_017001321.2:c.478+28T>C	XP_016856810.1:n.478+28T>C
NM_000530.8:c.448+28T>C MANE Select	NP_000521.2:n.448+28T>C
NM_001315491.2:c.448+28T>C	NP_001302420.1:n.448+28T>C