Canonical Allele Identifier: CA1202688018
Gene: MPZ HGNC NCBI

Linked Data

dbSNP Id: rs1670228276

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161305980_161305981insT , CM000663.2:g.161305980_161305981insT GRCh38
NC_000001.10:g.161275770_161275771insT , CM000663.1:g.161275770_161275771insT GRCh37
NC_000001.9:g.159542394_159542395insT NCBI36
NG_008055.1:g.8992_8993insA , LRG_256:g.8992_8993insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000526189.3:c.565-4_565-3insA ENSP00000488104.2:n.565-4_565-3insA
ENST00000533357.5:c.646-4_646-3insA MANE Select ENSP00000432943.1:n.646-4_646-3insA
ENST00000672287.2:c.58-4_58-3insA ENSP00000499818.2:n.58-4_58-3insA
ENST00000672602.2:c.646-4_646-3insA ENSP00000500814.2:n.646-4_646-3insA
ENST00000674861.1:n.709-4_709-3insA
ENST00000463290.5:c.646-4_646-3insA ENSP00000431538.1:n.646-4_646-3insA
ENST00000476410.1:n.232_233insA
ENST00000488271.1:n.84-4_84-3insA
ENST00000491222.5:c.58-4_58-3insA ENSP00000431441.1:n.58-4_58-3insA
ENST00000526189.2:c.309-4_309-3insA
ENST00000533357.4:c.646-4_646-3insA ENSP00000432943.1:n.646-4_646-3insA
NM_000530.6:c.646-4_646-3insA , LRG_256t1:c.646-4_646-3insA NP_000521.2:n.646-4_646-3insA
NM_000530.7:c.646-4_646-3insA NP_000521.2:n.646-4_646-3insA
NM_001315491.1:c.646-4_646-3insA NP_001302420.1:n.646-4_646-3insA
XM_017001321.2:c.675+127_675+128insA XP_016856810.1:n.675+127_675+128insA
NM_000530.8:c.646-4_646-3insA MANE Select NP_000521.2:n.646-4_646-3insA
NM_001315491.2:c.646-4_646-3insA NP_001302420.1:n.646-4_646-3insA