Canonical Allele Identifier: CA2574078229

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306632T>C , CM000663.2:g.161306632T>C	GRCh38
NC_000001.10:g.161276422T>C , CM000663.1:g.161276422T>C	GRCh37
NC_000001.9:g.159543046T>C	NCBI36
NG_008055.1:g.8341A>G , LRG_256:g.8341A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.367+157A>G	ENSP00000488104.2:n.367+157A>G
ENST00000533357.5:c.448+76A>G MANE Select	ENSP00000432943.1:n.448+76A>G
ENST00000672287.2:c.-141+76A>G	ENSP00000499818.2:n.-141+76A>G
ENST00000672602.2:c.448+76A>G	ENSP00000500814.2:n.448+76A>G
ENST00000674861.1:n.511+76A>G
ENST00000463290.5:c.448+76A>G	ENSP00000431538.1:n.448+76A>G
ENST00000491222.5:c.-141+76A>G	ENSP00000431441.1:n.-141+76A>G
ENST00000526189.2:c.111+157A>G
ENST00000533357.4:c.448+76A>G	ENSP00000432943.1:n.448+76A>G
NM_000530.6:c.448+76A>G , LRG_256t1:c.448+76A>G	NP_000521.2:n.448+76A>G
NM_000530.7:c.448+76A>G	NP_000521.2:n.448+76A>G
NM_001315491.1:c.448+76A>G	NP_001302420.1:n.448+76A>G
XM_017001321.2:c.478+76A>G	XP_016856810.1:n.478+76A>G
NM_000530.8:c.448+76A>G MANE Select	NP_000521.2:n.448+76A>G
NM_001315491.2:c.448+76A>G	NP_001302420.1:n.448+76A>G