Canonical Allele Identifier: CA382210522
Gene: MMP7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527869T>A , CM000673.2:g.102527869T>A GRCh38
NC_000011.9:g.102398600T>A , CM000673.1:g.102398600T>A GRCh37
NC_000011.8:g.101903810T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260227.5:c.223A>T MANE Select ENSP00000260227.4:p.Asn75Tyr
ENST00000260227.4:c.223A>T ENSP00000260227.4:p.Asn75Tyr
ENST00000531200.1:n.270A>T
ENST00000533366.5:n.273A>T
NM_002423.3:c.223A>T NP_002414.1:p.Asn75Tyr
NM_002423.4:c.223A>T NP_002414.1:p.Asn75Tyr
NM_002423.5:c.223A>T MANE Select NP_002414.1:p.Asn75Tyr