Canonical Allele Identifier: CA343348475

Gene: MPZ

Linked Data

• MyVariant Identifiers: chr1:g.161276524T>C (hg19) ; chr1:g.161306734T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306734T>C , CM000663.2:g.161306734T>C	GRCh38
NC_000001.10:g.161276524T>C , CM000663.1:g.161276524T>C	GRCh37
NC_000001.9:g.159543148T>C	NCBI36
NG_008055.1:g.8239A>G , LRG_256:g.8239A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.367+55A>G	ENSP00000488104.2:n.367+55A>G
ENST00000533357.5:c.422A>G MANE Select	ENSP00000432943.1:p.Gln141Arg
ENST00000672287.2:c.-167A>G	ENSP00000499818.2:n.-167A>G
ENST00000672602.2:c.422A>G	ENSP00000500814.2:p.Gln141Arg
ENST00000674861.1:n.485A>G
ENST00000463290.5:c.422A>G	ENSP00000431538.1:p.Gln141Arg
ENST00000491222.5:c.-167A>G	ENSP00000431441.1:n.-167A>G
ENST00000526189.2:c.111+55A>G
ENST00000533357.4:c.422A>G	ENSP00000432943.1:p.Gln141Arg
NM_000530.6:c.422A>G , LRG_256t1:c.422A>G	NP_000521.2:p.Gln141Arg
NM_000530.7:c.422A>G	NP_000521.2:p.Gln141Arg
NM_001315491.1:c.422A>G	NP_001302420.1:p.Gln141Arg
XM_017001321.2:c.452A>G	XP_016856810.1:p.Gln151Arg
NM_000530.8:c.422A>G MANE Select	NP_000521.2:p.Gln141Arg
NM_001315491.2:c.422A>G	NP_001302420.1:p.Gln141Arg