Canonical Allele Identifier: CA918955616
Gene: MMP7 HGNC NCBI

Linked Data

dbSNP Id: rs1555069611

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527862del , CM000673.2:g.102527862del GRCh38
NC_000011.9:g.102398593del , CM000673.1:g.102398593del GRCh37
NC_000011.8:g.101903803del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260227.5:c.230del MANE Select ENSP00000260227.4:p.Arg77ProfsTer3
ENST00000260227.4:c.230del ENSP00000260227.4:p.Arg77ProfsTer3
ENST00000531200.1:n.277del
ENST00000533366.5:n.280del
NM_002423.3:c.230del NP_002414.1:p.Arg77ProfsTer3
NM_002423.4:c.230del NP_002414.1:p.Arg77ProfsTer3
NM_002423.5:c.230del MANE Select NP_002414.1:p.Arg77ProfsTer3