Canonical Allele Identifier: CA2648773833
Gene: MPZ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161307038_161307039insAGAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAA , CM000663.2:g.161307038_161307039insAGAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000001.10:g.161276828_161276829insAGAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAA , CM000663.1:g.161276828_161276829insAGAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000001.9:g.159543452_159543453insAGAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAA NCBI36
NG_008055.1:g.7958_7959insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_256:g.7958_7959insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000526189.3:c.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000488104.2:n.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTT...
ENST00000533357.5:c.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000432943.1:n.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTT...
ENST00000672287.2:c.-354-94_-354-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000499818.2:n.-354-94_-354-93insCTTTTTTTTTTTTTTTTCTTTTT...
ENST00000672602.2:c.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000500814.2:n.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTT...
ENST00000674861.1:n.298-94_298-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000463290.5:c.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000431538.1:n.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTT...
ENST00000491222.5:c.-354-94_-354-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000431441.1:n.-354-94_-354-93insCTTTTTTTTTTTTTTTTCTTTTT...
ENST00000533357.4:c.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000432943.1:n.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTT...
NM_000530.6:c.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_256t1:c.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTT NP_000521.2:n.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTT...
NM_000530.7:c.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTT NP_000521.2:n.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTT...
NM_001315491.1:c.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTT NP_001302420.1:n.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTT...
XM_017001321.2:c.265-94_265-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTT XP_016856810.1:n.265-94_265-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTT...
NM_000530.8:c.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_000521.2:n.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTT...
NM_001315491.2:c.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTT NP_001302420.1:n.235-94_235-93insCTTTTTTTTTTTTTTTTCTTTTTTTTTT...