Canonical Allele Identifier: CA1202688152

Gene: MPZ

Linked Data

• dbSNP Id: rs1670231592

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306072_161306073insA , CM000663.2:g.161306072_161306073insA	GRCh38
NC_000001.10:g.161275862_161275863insA , CM000663.1:g.161275862_161275863insA	GRCh37
NC_000001.9:g.159542486_159542487insA	NCBI36
NG_008055.1:g.8900_8901insT , LRG_256:g.8900_8901insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.564+35_564+36insT	ENSP00000488104.2:n.564+35_564+36insT
ENST00000533357.5:c.645+35_645+36insT MANE Select	ENSP00000432943.1:n.645+35_645+36insT
ENST00000672287.2:c.57+35_57+36insT	ENSP00000499818.2:n.57+35_57+36insT
ENST00000672602.2:c.645+35_645+36insT	ENSP00000500814.2:n.645+35_645+36insT
ENST00000674861.1:n.708+35_708+36insT
ENST00000463290.5:c.645+35_645+36insT	ENSP00000431538.1:n.645+35_645+36insT
ENST00000476410.1:n.140_141insT
ENST00000488271.1:n.83+35_83+36insT
ENST00000491222.5:c.57+35_57+36insT	ENSP00000431441.1:n.57+35_57+36insT
ENST00000526189.2:c.308+35_308+36insT
ENST00000533357.4:c.645+35_645+36insT	ENSP00000432943.1:n.645+35_645+36insT
NM_000530.6:c.645+35_645+36insT , LRG_256t1:c.645+35_645+36insT	NP_000521.2:n.645+35_645+36insT
NM_000530.7:c.645+35_645+36insT	NP_000521.2:n.645+35_645+36insT
NM_001315491.1:c.645+35_645+36insT	NP_001302420.1:n.645+35_645+36insT
XM_017001321.2:c.675+35_675+36insT	XP_016856810.1:n.675+35_675+36insT
NM_000530.8:c.645+35_645+36insT MANE Select	NP_000521.2:n.645+35_645+36insT
NM_001315491.2:c.645+35_645+36insT	NP_001302420.1:n.645+35_645+36insT