Canonical Allele Identifier: CA343344665
Gene: MPZ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161306120C>A , CM000663.2:g.161306120C>A GRCh38
NC_000001.10:g.161275910C>A , CM000663.1:g.161275910C>A GRCh37
NC_000001.9:g.159542534C>A NCBI36
NG_008055.1:g.8853G>T , LRG_256:g.8853G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000526189.3:c.552G>T ENSP00000488104.2:p.Lys184Asn
ENST00000533357.5:c.633G>T MANE Select ENSP00000432943.1:p.Lys211Asn
ENST00000672287.2:c.45G>T ENSP00000499818.2:p.Lys15Asn
ENST00000672602.2:c.633G>T ENSP00000500814.2:p.Lys211Asn
ENST00000674861.1:n.696G>T
ENST00000463290.5:c.633G>T ENSP00000431538.1:p.Lys211Asn
ENST00000476410.1:n.93G>T
ENST00000488271.1:n.71G>T
ENST00000491222.5:c.45G>T ENSP00000431441.1:p.Lys15Asn
ENST00000526189.2:c.296G>T
ENST00000533357.4:c.633G>T ENSP00000432943.1:p.Lys211Asn
NM_000530.6:c.633G>T , LRG_256t1:c.633G>T NP_000521.2:p.Lys211Asn
NM_000530.7:c.633G>T NP_000521.2:p.Lys211Asn
NM_001315491.1:c.633G>T NP_001302420.1:p.Lys211Asn
XM_017001321.2:c.663G>T XP_016856810.1:p.Lys221Asn
NM_000530.8:c.633G>T MANE Select NP_000521.2:p.Lys211Asn
NM_001315491.2:c.633G>T NP_001302420.1:p.Lys211Asn