Canonical Allele Identifier: CA382209652
Gene: MMP7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527789G>T , CM000673.2:g.102527789G>T GRCh38
NC_000011.9:g.102398520G>T , CM000673.1:g.102398520G>T GRCh37
NC_000011.8:g.101903730G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260227.5:c.303C>A MANE Select ENSP00000260227.4:p.Ser101Arg
ENST00000260227.4:c.303C>A ENSP00000260227.4:p.Ser101Arg
ENST00000531200.1:n.350C>A
ENST00000533366.5:n.353C>A
NM_002423.3:c.303C>A NP_002414.1:p.Ser101Arg
NM_002423.4:c.303C>A NP_002414.1:p.Ser101Arg
NM_002423.5:c.303C>A MANE Select NP_002414.1:p.Ser101Arg