Canonical Allele Identifier: CA382210552
Gene: MMP7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527871A>C , CM000673.2:g.102527871A>C GRCh38
NC_000011.9:g.102398602A>C , CM000673.1:g.102398602A>C GRCh37
NC_000011.8:g.101903812A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260227.5:c.221T>G MANE Select ENSP00000260227.4:p.Leu74Ter
ENST00000260227.4:c.221T>G ENSP00000260227.4:p.Leu74Ter
ENST00000531200.1:n.268T>G
ENST00000533366.5:n.271T>G
NM_002423.3:c.221T>G NP_002414.1:p.Leu74Ter
NM_002423.4:c.221T>G NP_002414.1:p.Leu74Ter
NM_002423.5:c.221T>G MANE Select NP_002414.1:p.Leu74Ter