Canonical Allele Identifier: CA343343816
Gene: MPZ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161305889T>C , CM000663.2:g.161305889T>C GRCh38
NC_000001.10:g.161275679T>C , CM000663.1:g.161275679T>C GRCh37
NC_000001.9:g.159542303T>C NCBI36
NG_008055.1:g.9084A>G , LRG_256:g.9084A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000526189.3:c.653A>G ENSP00000488104.2:p.Lys218Arg
ENST00000533357.5:c.734A>G MANE Select ENSP00000432943.1:p.Lys245Arg
ENST00000672287.2:c.146A>G ENSP00000499818.2:p.Lys49Arg
ENST00000672602.2:c.734A>G ENSP00000500814.2:p.Lys245Arg
ENST00000674861.1:n.797A>G
ENST00000463290.5:c.734A>G ENSP00000431538.1:p.Lys245Arg
ENST00000476410.1:n.324A>G
ENST00000488271.1:n.172A>G
ENST00000491222.5:c.146A>G ENSP00000431441.1:p.Lys49Arg
ENST00000526189.2:c.397A>G
ENST00000533357.4:c.734A>G ENSP00000432943.1:p.Lys245Arg
NM_000530.6:c.734A>G , LRG_256t1:c.734A>G NP_000521.2:p.Lys245Arg
NM_000530.7:c.734A>G NP_000521.2:p.Lys245Arg
NM_001315491.1:c.734A>G NP_001302420.1:p.Lys245Arg
XM_017001321.2:c.675+219A>G XP_016856810.1:n.675+219A>G
NM_000530.8:c.734A>G MANE Select NP_000521.2:p.Lys245Arg
NM_001315491.2:c.734A>G NP_001302420.1:p.Lys245Arg