Canonical Allele Identifier: CA1008409341
Gene: MPZ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161307018_161307019insCA , CM000663.2:g.161307018_161307019insCA GRCh38
NC_000001.10:g.161276808_161276809insCA , CM000663.1:g.161276808_161276809insCA GRCh37
NC_000001.9:g.159543432_159543433insCA NCBI36
NG_008055.1:g.7955_7956insGT , LRG_256:g.7955_7956insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000526189.3:c.235-97_235-96insGT ENSP00000488104.2:n.235-97_235-96insGT
ENST00000533357.5:c.235-97_235-96insGT MANE Select ENSP00000432943.1:n.235-97_235-96insGT
ENST00000672287.2:c.-354-97_-354-96insGT ENSP00000499818.2:n.-354-97_-354-96insGT
ENST00000672602.2:c.235-97_235-96insGT ENSP00000500814.2:n.235-97_235-96insGT
ENST00000674861.1:n.298-97_298-96insGT
ENST00000463290.5:c.235-97_235-96insGT ENSP00000431538.1:n.235-97_235-96insGT
ENST00000491222.5:c.-354-97_-354-96insGT ENSP00000431441.1:n.-354-97_-354-96insGT
ENST00000533357.4:c.235-97_235-96insGT ENSP00000432943.1:n.235-97_235-96insGT
NM_000530.6:c.235-97_235-96insGT , LRG_256t1:c.235-97_235-96insGT NP_000521.2:n.235-97_235-96insGT
NM_000530.7:c.235-97_235-96insGT NP_000521.2:n.235-97_235-96insGT
NM_001315491.1:c.235-97_235-96insGT NP_001302420.1:n.235-97_235-96insGT
XM_017001321.2:c.265-97_265-96insGT XP_016856810.1:n.265-97_265-96insGT
NM_000530.8:c.235-97_235-96insGT MANE Select NP_000521.2:n.235-97_235-96insGT
NM_001315491.2:c.235-97_235-96insGT NP_001302420.1:n.235-97_235-96insGT