Canonical Allele Identifier: CA382208879
Gene: MMP7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527662A>C , CM000673.2:g.102527662A>C GRCh38
NC_000011.9:g.102398393A>C , CM000673.1:g.102398393A>C GRCh37
NC_000011.8:g.101903603A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260227.5:c.346T>G MANE Select ENSP00000260227.4:p.Tyr116Asp
ENST00000260227.4:c.346T>G ENSP00000260227.4:p.Tyr116Asp
ENST00000531200.1:n.393T>G
ENST00000533366.5:n.396T>G
NM_002423.3:c.346T>G NP_002414.1:p.Tyr116Asp
NM_002423.4:c.346T>G NP_002414.1:p.Tyr116Asp
NM_002423.5:c.346T>G MANE Select NP_002414.1:p.Tyr116Asp