Canonical Allele Identifier: CA227293319
Gene: MMP7 HGNC NCBI

Linked Data

dbSNP Id: rs879695651

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527861_102527862delinsT , CM000673.2:g.102527861_102527862delinsT GRCh38
NC_000011.9:g.102398592_102398593delinsT , CM000673.1:g.102398592_102398593delinsT GRCh37
NC_000011.8:g.101903802_101903803delinsT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260227.5:c.230_231delinsA MANE Select ENSP00000260227.4:p.Arg77GlnfsTer3
ENST00000260227.4:c.230_231delinsA ENSP00000260227.4:p.Arg77GlnfsTer3
ENST00000531200.1:n.277_278delinsA
ENST00000533366.5:n.280_281delinsA
NM_002423.3:c.230_231delinsA NP_002414.1:p.Arg77GlnfsTer3
NM_002423.4:c.230_231delinsA NP_002414.1:p.Arg77GlnfsTer3
NM_002423.5:c.230_231delinsA MANE Select NP_002414.1:p.Arg77GlnfsTer3