Canonical Allele Identifier: CA382210468
Gene: MMP7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527865G>T , CM000673.2:g.102527865G>T GRCh38
NC_000011.9:g.102398596G>T , CM000673.1:g.102398596G>T GRCh37
NC_000011.8:g.101903806G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260227.5:c.227C>A MANE Select ENSP00000260227.4:p.Ser76Tyr
ENST00000260227.4:c.227C>A ENSP00000260227.4:p.Ser76Tyr
ENST00000531200.1:n.274C>A
ENST00000533366.5:n.277C>A
NM_002423.3:c.227C>A NP_002414.1:p.Ser76Tyr
NM_002423.4:c.227C>A NP_002414.1:p.Ser76Tyr
NM_002423.5:c.227C>A MANE Select NP_002414.1:p.Ser76Tyr