Canonical Allele Identifier: CA382208887
Gene: MMP7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527667A>G , CM000673.2:g.102527667A>G GRCh38
NC_000011.9:g.102398398A>G , CM000673.1:g.102398398A>G GRCh37
NC_000011.8:g.101903608A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260227.5:c.341T>C MANE Select ENSP00000260227.4:p.Val114Ala
ENST00000260227.4:c.341T>C ENSP00000260227.4:p.Val114Ala
ENST00000531200.1:n.388T>C
ENST00000533366.5:n.391T>C
NM_002423.3:c.341T>C NP_002414.1:p.Val114Ala
NM_002423.4:c.341T>C NP_002414.1:p.Val114Ala
NM_002423.5:c.341T>C MANE Select NP_002414.1:p.Val114Ala