Canonical Allele Identifier: CA382210616
Gene: MMP7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527875T>G , CM000673.2:g.102527875T>G GRCh38
NC_000011.9:g.102398606T>G , CM000673.1:g.102398606T>G GRCh37
NC_000011.8:g.101903816T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260227.5:c.217A>C MANE Select ENSP00000260227.4:p.Met73Leu
ENST00000260227.4:c.217A>C ENSP00000260227.4:p.Met73Leu
ENST00000531200.1:n.264A>C
ENST00000533366.5:n.267A>C
NM_002423.3:c.217A>C NP_002414.1:p.Met73Leu
NM_002423.4:c.217A>C NP_002414.1:p.Met73Leu
NM_002423.5:c.217A>C MANE Select NP_002414.1:p.Met73Leu