Canonical Allele Identifier: CA382210477
Gene: MMP7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527866A>G , CM000673.2:g.102527866A>G GRCh38
NC_000011.9:g.102398597A>G , CM000673.1:g.102398597A>G GRCh37
NC_000011.8:g.101903807A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260227.5:c.226T>C MANE Select ENSP00000260227.4:p.Ser76Pro
ENST00000260227.4:c.226T>C ENSP00000260227.4:p.Ser76Pro
ENST00000531200.1:n.273T>C
ENST00000533366.5:n.276T>C
NM_002423.3:c.226T>C NP_002414.1:p.Ser76Pro
NM_002423.4:c.226T>C NP_002414.1:p.Ser76Pro
NM_002423.5:c.226T>C MANE Select NP_002414.1:p.Ser76Pro